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Posts
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- eConsent: Definitions & Details
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Beyond Numbers: One Family’s Clinical Trial Journey (Part 1)
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Does Greater Patient Control of Healthcare Data Impact Clinical Trials?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Introduces eTMF Master for Electronic Trial Master File Management in Clinical Studies
- Anju Launches New CRO Partner Program
- Anju sets up COVID treatment study build in record 10 days using its eClinical Suite
- Anju Software Launches a Web-based Coding System
- Anju Software Launches First-of-its-Kind RTSM Randomization Simulator for Optimized Clinical Study Design
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju Software Sets New Standard for Reducing Clinical Study Build Times with TrialMaster 5.1: Release Offers New Proprietary Technology Enabling Reuse of Edit Checks Across Multiple Clinical Trials
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- FGK Clinical Research Signs Five-Year Agreement with OmniComm Systems for Multiple eClinical Products
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- Gustave Roussy Renews TrialMaster EDC Agreement with Anju Software to Accelerate Complex Oncology Clinical Studies
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- OmniComm’s IRTMaster Features Configurable, Pre-Validated Modules to Accelerate Trial Development
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Annual DMB Conference in Paris This November: Celebrating 25 Years
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Can’t-Miss Presenters And Talks at the 6th European Conference on Clinical Research
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- DIA’s Global Clinical Trial Disclosure and Data Transparency Conference
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Insights from DIA 2019 Global Annual Meeting
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Join Anju Software at DIA 2021 Global Annual Meeting for Best Practices in Utilizing Clinical Trial and Medical Affairs Technology
- Join Anju Software at DIA China for Best Practices in Utilizing Clinical Trial Technology
- Join Anju Software at OCT Europe for Best Practices in Utilizing Decentralized Trials Technology
- Join Anju Software at OCT West Coast for Best Practices in Decentralized Trials Technology – recording in link below
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- Message to Clients – COVID-19
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- OCT Europe 2022: A Preview
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- SCOPE Summit 2020: Discover Anju’s eClinical Software Solutions
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- There is no other event like DIA 2019 Global Annual Meeting
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Top Events and Speakers at the DIA 2022 Global Annual Meeting
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- Visit us at The PharmaSUG 2019: June 16-19 in Philadelphia
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
eClinical
- 10 Reasons Why We Must Integrate EMR and EDC
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Ways to Improve the Security of Clinical Trial Data
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Configurability and Customization: Key Features in an eTMF Solution
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How AI and Machine Learning Are Reshaping Clinical Trials
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How More Data Can Lead to Shorter Clinical Trials
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Prepare a Successful NDA Submission
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Clinical Oversight Solutions Effectively
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- Optimize Clinical Study Design With Randomization Simulation
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- SCOPE 2023 Conference Preview
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Your eTMF Needs Role-Based Access
- World-Class EDC for World-Class Cancer Research Center
Insights
- 10 Global Medical Affairs Conferences to Attend in 2020
- 10 Medical Affairs Conferences in Late 2020 and Early 2021
- 10 Reasons Why We Must Integrate EMR and EDC
- 2019 Exhibitions and Events: Important Healthcare IT Conferences
- 21st Century Cures Act: Effects on Informed Consent Requirements in Clinical Trials
- 3 Legal Questions That Will Define the Frontiers of Clinical Research
- 4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials
- 4 Ways an IRMS Helps Medical Affairs Manage and Share Insights
- 5 Major Pitfalls in Clinical Trial Design and How to Avoid Them
- 5 Skills That Tomorrow’s Data Managers Will Need to Succeed
- 5 Things Medical Affairs Can Do to Support Late Life Cycle Drugs
- 5 Tips to Better Engage With Digital Opinion Leaders
- 5 Ways to Improve the Security of Clinical Trial Data
- A Global Approach: Clinical Trials in Emerging Markets
- A Look at the Future of Decentralized Trials: Predictions from Anju Software’s EVP of Operations, Mike Keens
- Achieving Transparency: Why and How to Share Trial Results Data
- Adaptive Design for Clinical Trials: Best Practice For Managing Phase Transition
- Analysis performed by Anju Software via ta-Scan on COVID-19
- Anju Innovation Forum Day 2 Highlights
- Anju Innovation Forum Day 3 Highlights
- Anju Software Provides Adaptive Technology Solutions For Clinical Trials And Medical Affairs
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Anju’s EVP of Operations Mike Keens Guest on Applied Clinical Trials Podcast
- Automated Clinical Data Exchange Can Boost Collaboration and Clinical Trial Success
- Automation, Analytics, AI and the Future of Trial Monitoring
- Best Practices of Medical Affairs Publication Planning in 2021
- Big Data, Big Benefits: How Third Party Data Can Improve Clinical Trials
- Breaking Down Data Silos in Life Sciences
- Building a Strong Foundation for Medical Affairs Leadership
- Building Opinion Leader Relationships in a Post-Pandemic World
- Can’t-Miss Presenters And Talks at the 6th European Conference on Clinical Research
- Chronic Obstructive Pulmonary Disease: Latest Clinical Data
- Clinical Data Management and the Rise of Healthcare-Related Cyberattacks
- Clinical Data Management: Artificial Intelligence and Machine Learning
- Clinical Trial Data Privacy: What Trial Managers Need to Know
- Clinical Trial Data Sharing: What Medical Affairs Teams Need to Do
- Clinical Trial Incentives: The Bias Problem in a Self-Selecting Populace
- Clinical Trial Reimbursement for Patients: Current Challenges and Future Improvements
- Clinical Trial Under-Enrollment: How to Prevent It
- Collaboration Opportunities Between Regulators and Medical Affairs
- Configurability and Customization: Key Features in an eTMF Solution
- Coronavirus: The Role of Medical Affairs Teams in Public Health
- COVID-19 Has Reaffirmed the Importance of Clear, Accessible Science
- COVID-19 Transforms the Clinical Trial Industry Ecosystem | IndustryWired
- COVID-19 Vaccine Development Enables CROs to Optimize Processes
- Current Event Analysis: Brexit, Clinical Trials and Regulations
- Data Interoperability and Data Sharing: Do They Work in Practice?
- Data Protection in Medical Affairs: A Guide to Basic Cybersecurity
- Data Protection Officers and Clinical Trials: What CROs Need to Know
- Decentralized Clinical Trials: Bridging the Distance During COVID-19
- Digital Doctors: How To Improve Virtual Bedside Manner in Clinical Trials
- Do No Harm: How to Mitigate Risk in Child and FIH Clinical Trials
- Does Your Clinical Trial Need a Chief Patient Experience Officer?
- Drug Labeling Trends: Making Medical Language Accessible to Patients
- dTrial Forum in Nanjing, China hosts Feng Cheng as speaker
- Early-Stage Decentralized Clinical Trial Site Selection: Key Factors
- Ease of Implementation and Customization Spell eTMF Success
- Engagement and Adherence: How Technology is Keeping Trial Patients in the Loop
- Evolving Needs for CROs: Understanding FDA Expectations
- Experimental Design: New Therapies Are Being Developed to Treat Lifelong Illness
- Expert Hire: Profiles of 5 Top Clinical Research Recruitment Agencies
- Faster Than Ever: The Evolution of Clinical Trials
- FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?
- Find and Keep: How Directors Can Attract and Develop Strong Clinical Research Associates
- Forbes Ranks Virtual Trials as a Top 5 Digital Health Technology Trend
- Geriatric Research: Why Your Study Should Include More Seniors
- Getting the Most Out of Your EDC Software
- Global Clinical Trials: Managing Patients and Meeting Compliance
- How a Real-Time eTMF Dashboard Helps Keep a Trial on Track
- How a Unified Data Platform Improves Clinical Trial Procedures and Outcomes
- How AI and Machine Learning Are Reshaping Clinical Trials
- How AI, Machine Learning, and Clinical Intelligence Are Improving Oncology Research
- How Clinical Research as a Care Option can Improve Patient Outcomes
- How Clinical Trial Organizations Can Convey Trust and Credibility
- How Contract Research Organizations Are Adapting to Virtual Trials
- How CROs Can Benefit from Continual Improvement Analysis and Benchmarking
- How CTM Software Can Improve Site Selection For Clinical Trials
- How Decentralized Trials Combat Unconscious Bias and Reach More Diverse Patient Groups
- How Do Clinical Trial Recruitment Incentives Bias Research Outcomes?
- How Do We Solve Pharma’s Data Dysfunction Conundrum?
- How Efficiencies in Trial Builds Facilitate Quicker Data Collection
- How Electronic Data Capture Software Facilitates Cleaner Trial Data
- How GDPR is Affecting Clinical Trials
- How Historical Data and Controls Improve Clinical Trials
- How Is the Role of Clinical Data Manager Changing and Why
- How Medical Affairs Can Amplify the Patient Voice
- How Medical Affairs Can Provide Credible Information to Consumers
- How Medical Affairs Can Support a Product Against New Competition
- How Medical Affairs Can Support Pharma Marketing
- How Medical Affairs Can Use Tech to Provide Medical Information Letters
- How Medical Affairs Teams Are Affected by Cybersecurity and Data Privacy Issues
- How Medical Affairs Teams Can Advocate for Patient-Centric Healthcare
- How Medical Affairs Teams Can Boost Stakeholder Engagement
- How Medical Affairs Teams Can Help Get Off-Label Drugs to Patients
- How Medical Affairs Teams Can Improve Their Digital Communications
- How Medical Affairs Teams Can Optimize Product Life Cycle
- How Medical Affairs Teams Can Promote Value-Based Clinical Trials
- How Medical Science Liaisons Should Engage With Key Opinion Leaders
- How More Data Can Lead to Shorter Clinical Trials
- How MSLs Became Pharma’s Essential Information Contact Point
- How Patient Privacy and Cybersecurity Affect Remote Clinical Trials
- How Researchers Address Patient Tech Fatigue in Decentralized Trials
- How Risk-Based Monitoring Can Improve Clinical Trial Operations
- How Tech Can Streamline Communication Between Clinical Trial Sites, Sponsors and CROs
- How Technology is Moving Decentralized Clinical Trials Forward
- How the COVID-19 Pandemic Changed Data Collection in Clinical Trials
- How the COVID-19 Vaccine Will Change the Role of Medical Affairs Teams
- How The Evolving Clinical Trial Ecosystem Is Changing Stakeholder Relationships
- How the Right Tools Make Clinical Data Integration Seamless
- How to Achieve CTMS Best Practices: Train Your Staff
- How to Best Ensure Accuracy in Coding for Clinical Trials
- How to Build Flexible Clinical Trial Design — and How Software Can Help
- How to Create an Effective Risk-Based Monitoring Plan
- How to Create Social Media Content to Engage Clinical Trials Patients
- How to Design Patient-Friendly Trials and Improve Site Performance
- How to Discuss Clinical Trial Performance Metrics with Stakeholders
- How To Empower Medical Science Liaisons With Data, and Why You Should
- How to Engage Primary Care Providers in Clinical Trials and Connect With Patients Who Don’t Have Them
- How to Foster Positive Relationships with Patient Advocates — and Why It’s Important
- How to Improve Patient Retention in Clinical Trials
- How To Improve the Process of Adverse Event Reporting
- How to Improve the Use of EHRs for a More Efficient Clinical Trial
- How to Improve Trial Site Relationships for More Efficient Trials
- How to Manage Patient Fear Regarding Clinical Trial Risks
- How to Measure the Effectiveness of Medical Information Distribution
- How to Prepare a Successful NDA Submission
- How To Prevent Systemic Bias in Clinical Trials
- How to Simplify the Clinical Trial Regulatory Submission Process
- How To Use Adaptive Systems to Get the Most from Decentralized Trials
- How to Use Anju Software’s Pubstrat MAX to Better Promote Your Clinical Trial & Therapy Performance Results
- How to Use Clinical Oversight Solutions Effectively
- How Trial Managers Can Increase Diversity in Clinical Trials
- How Will COVID-19 Impact Clinical Trials in the Long Term?
- Improve Clinical Trial Management with Automated CTMS Tools
- Improve Clinical Trial Planning With Screening and Randomization
- In a Data-Rich Landscape, a Single Source of Truth is Key
- Informed Site Selection is Mission Critical in Post COVID-19 Era
- Insights from CBI’s Medical Publications and Communications Forum
- INSIGHTS from DIA 2019 MICC
- INSIGHTS from ISMPP EU
- International Research Collaboration: What Tools Can Help
- Is There a Place for Integrative Medicine Approaches in Clinical Trials?
- Lightening the Load: Reducing Patient Burden in Clinical Trials
- Machine Learning and KOL Networks: The Future of Medical Affairs
- Maintain Remote Professional Relationships: 3 Tips for Medical Affairs
- Medical Affairs KPIs: How to Create a Framework For Measuring Success
- Mental Health Clinical Trials: Controversies, Challenges, Solutions
- More than Reduced Costs: The Benefits of Remote Monitoring in Clinical Trials
- New Shifts In The Medical Affairs Ecosystem
- New Technology & the Global COVID Pandemic Drive the Need for More Decentralized Trials
- Our Most Anticipated Events at DIA MASC 2023
- Outsourcing Clinical Trials: How to Build Successful Partnerships
- Overcoming Accessibility Challenges in International Clinical Trials
- Overcoming Language and Culture Barriers in Multinational Clinical Trials
- Pandemic-Driven Medical Affairs and Scientific Insights Management
- Partnering with Patient Advocacy Groups Benefits Pharma and Patients
- Patient-Centric Approach in Clinical Trial Design: Involve Patients Early
- Patients as Partners: The Value of Post-Trial Communication
- Precision Medicine: Its Impact on Clinical Trials and Orphan Drugs
- Price Check: How to Cut Costs in Clinical Trials
- Public Health Misinformation: What Can Medical Affairs Teams Do?
- Publicizing Research: Reach Audiences and Combat Misinformation
- Rare Disease Clinical Trials: How to Improve Participation and Outcomes
- Research During a Pandemic: Trial Leadership Supporting Their Teams
- Researchers Whose Work May Lead to Cancer Treatment Breakthroughs
- Rethinking the Clinical Data Ecosystem When Managing Multiple Sources
- Science Behind the Comms: How MA Teams Add Value to Messaging
- SCOPE 2023 Conference Preview
- Share Research, Build Trust: Medical Affairs Leads COVID-19 Response
- Social Media for Clinical Trial Recruitment | Advertising Strategies
- Strategies for More Accurate Clinical Trial Forecasting and Budgeting
- Support for Awareness Campaigns: Good for Pharma and Patients
- TA Scan Won SCOPE Best of Show Award
- Tech Skills and Digital Natives in Demand as Clinical Trial Industry Evolves
- The Benefits of Standardized, Machine-Readable Clinical Data
- The Continuing Rise of Decentralized Clinical Trials
- The Emerging Role of Medical Science Liaisons on Medical Affairs Teams
- The Emerging Role of Voice Tech and Wearables in Clinical Trials
- The Future of Decentralized Trials
- The Importance of User Experience in Life Sciences Software
- The Mental Health Impact of COVID-19 And How MA Teams Can Help
- The Next Step: Using AI to Formulate Clinical Trial Research Questions
- The Next Step: Using AI to Formulate Clinical Trial Research Questions
- The Post-Pandemic Future of Medical Information Call Centers
- The Present and Future of Synthetic Data
- The Project Management Frameworks and Tools Shaping Clinical Trials
- The Requirements of an Effective Electronic Data Capture System (EDCS)
- The Right Tool for EDC
- The Rise of the Digital Opinion Leader in Post-COVID Medical Affairs
- The Role of Electronic Data Capture in Decentralized Trials
- The Role of Medical Affairs in Combating Misinformation
- The Role of Nurse Navigators in Oncology Trials
- The State of Clinical Research During the COVID-19 Pandemic
- The Ugly Truth About Paper Diaries
- Three Ways Decentralized Trials Bolster Patient Recruitment
- To Catch a Predator: Best Practices for Uncovering Predatory Journals and Conferences
- Top 2020 Conferences CROs Should Not Miss
- Top KPIs for Measuring Medical Affairs Success in 2022
- Tracking Relationships: Understanding KPIs That Measure KOL Engagement
- Trial Eligibility Criteria: The Problem with Current Exclusion Strategies
- Trial Participant Retention: Maintaining Adherence, Minimizing Dropout
- Trust-building in a Pandemic: Collaborative Strategies for MA teams
- Understanding Attrition: Gleaning Insights From Patients Who Quit
- Understanding Cross-Border Enrollment for International Clinical Trials
- Understanding FDA 483: How To Run a Compliant Trial Every Time
- Understanding HHS’ Proposed Rule Changes to HIPAA
- Understanding Risk-Based Clinical Quality Management Technology
- Understanding Roles and Needs of Stakeholders in Decentralized Trials
- Understanding Security and Role-Based Access in an eTMF Platform
- Understanding the Changing Face of Early Phase Clinical Trials
- Understanding the Value of Blockchain for Clinical Trial Data
- Understanding Which KOLs are Key for You
- Update on Analysis performed by Anju Software via ta-Scan on COVID-19
- Video Interview: How is the Global Oncology Community Using Technology to Keep Clinical Trials Going?
- Virtual Clinical Trials: The Patient Engagement Benefits & Challenges
- Virtual Reality in Clinical Research: Potential, Implementation and Challenges
- What Challenges Face Researchers With Direct-To-Patient Trials
- What Clinical Trial Leaders Need to Know About Using Synthetic Data
- What Extra Support Should Clinical Research Teams Offer Participants?
- What Five Key Features Should a Trial Director Look for in an EDC?
- What Google’s Entrance Into Healthcare Data Means for Clinical Trials
- What Happens When Medical Affairs Intersects with Politics?
- What is the Role of Synthetic Data in Early-Phase Clinical Trials?
- What to Consider When Adopting New Technology in Clinical Trial
- What To Look For in a Medical Affairs Customer Relationship Management Platform
- What To Look For in an eTMF
- When a Direct-to-Patient Trial Model Is the Right Choice
- Why an eTMF? It’s Time for a Specialized Digital Solution
- Why CRO Staff Need Robust Digital Literacy Skills
- Why Decentralized Clinical Trials Are the Future in a Post-COVID World
- Why Diverse Clinical Trials Are Essential for Personalized Medicine
- Why Life Sciences Companies Need Regular Medical Affairs Audits
- Why Medical Affairs Must Lead a Patient-Centric Approach to R&D
- Why Time Management is Essential for Clinical Trials
- Why Your eTMF Needs Role-Based Access
- Women in Clinical Trials: More Than Equal Representation is Required
- Working With Disparate Data Sources To Improve Your Trials
- World Multiple Sclerosis Day: Data Analysis on the Latest Clinical Research
- World Parkinson’s Day: Data Analysis on the Latest Clinical Research
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- You’ve Collected Your Medical Affairs Data. Now What?
Medical Affairs
- 10 Global Medical Affairs Conferences to Attend in 2020
- 10 Medical Affairs Conferences in Late 2020 and Early 2021
- 15th Annual CBI Medical Publications and Communications Forum
- 17th Annual Meeting of ISMPP 2021
- 2019 European Meeting of ISMPP
- 2020 European Meeting of ISMPP – Precision Communication: Achieving Clarity, Reach and Value
- 4 Ways an IRMS Helps Medical Affairs Manage and Share Insights
- 5 Things Medical Affairs Can Do to Support Late Life Cycle Drugs
- 5 Tips to Better Engage With Digital Opinion Leaders
- Anju Discusses Medical Information Call Center Adaptation Pre & Current COVID at DIA
- Anju Leads Session On Virtual Medical Content Compliance, Previews pubstrat max Technology at TIPPA
- Anju Software is a Proud Sponsor of DIA Medical Affairs and Scientific Communications (MASC) Forum
- Anju’s CEO Laurence Birch Interviewed by Insights Success: Delivering Adaptive Life Sciences Technology
- Best Practices of Medical Affairs Publication Planning in 2021
- Building a Strong Foundation for Medical Affairs Leadership
- Building Opinion Leader Relationships in a Post-Pandemic World
- Clinical Trial Data Sharing: What Medical Affairs Teams Need to Do
- Collaboration Opportunities Between Regulators and Medical Affairs
- Come visit us at the TIPPA Conference in San Diego
- Coronavirus: The Role of Medical Affairs Teams in Public Health
- Data Protection in Medical Affairs: A Guide to Basic Cybersecurity
- DIA 12th Annual European Medical Information and Communications Conference and Exhibition
- DIA Medical Information and Communications Conference
- Drug Labeling Trends: Making Medical Language Accessible to Patients
- How AI, Machine Learning, and Clinical Intelligence Are Improving Oncology Research
- How Big Data and AI Are Changing the Role of Medical Affairs
- How Medical Affairs Can Amplify the Patient Voice
- How Medical Affairs Can Provide Credible Information to Consumers
- How Medical Affairs Can Support a Product Against New Competition
- How Medical Affairs Can Support Pharma Marketing
- How Medical Affairs Can Use Tech to Provide Medical Information Letters
- How Medical Affairs Teams Are Affected by Cybersecurity and Data Privacy Issues
- How Medical Affairs Teams Can Advocate for Patient-Centric Healthcare
- How Medical Affairs Teams Can Boost Stakeholder Engagement
- How Medical Affairs Teams Can Help Get Off-Label Drugs to Patients
- How Medical Affairs Teams Can Improve Their Digital Communications
- How Medical Affairs Teams Can Optimize Product Life Cycle
- How Medical Affairs Teams Can Promote Value-Based Clinical Trials
- How Medical Science Liaisons Should Engage With Key Opinion Leaders
- How MSLs Became Pharma’s Essential Information Contact Point
- How the COVID-19 Vaccine Will Change the Role of Medical Affairs Teams
- How To Empower Medical Science Liaisons With Data, and Why You Should
- How to Measure the Effectiveness of Medical Information Distribution
- How to Use Anju Software’s Pubstrat MAX to Better Promote Your Clinical Trial & Therapy Performance Results
- Insights from CBI’s Medical Publications and Communications Forum
- INSIGHTS from DIA 2019 MICC
- ISMPP EU Virtual Conference 2021
- ISMPP West 2019 – Changing Tides and Technology in Scientific Communications
- ISMPP West 2021: All Hands on Deck: Opportunities for Connectivity, Transparency, and Inclusivity
- Join Anju Software at Pharma Europe 2021 for a Presentation on Empowering Your MSLs with the Power of Data
- Join us in sunny San Diego as ISMPP heads West for first meeting in the historic Gas Lamp Quarter
- Machine Learning and KOL Networks: The Future of Medical Affairs
- Maintain Remote Professional Relationships: 3 Tips for Medical Affairs
- MAPS Annual Meeting 2019 – Not just a one-time event…
- MASS West 2019 – Medical Affairs Strategic Summit
- Medical Affairs KPIs: How to Create a Framework For Measuring Success
- New Shifts In The Medical Affairs Ecosystem
- Notable Speakers: DIA Medical Information Conference
- Pandemic-Driven Medical Affairs and Scientific Insights Management
- Public Health Misinformation: What Can Medical Affairs Teams Do?
- Publicizing Research: Reach Audiences and Combat Misinformation
- Researchers Whose Work May Lead to Cancer Treatment Breakthroughs
- Science Behind the Comms: How MA Teams Add Value to Messaging
- Share Research, Build Trust: Medical Affairs Leads COVID-19 Response
- TA Scan Won SCOPE Best of Show Award
- The Emerging Role of Medical Science Liaisons on Medical Affairs Teams
- The Mental Health Impact of COVID-19 And How MA Teams Can Help
- The Post-Pandemic Future of Medical Information Call Centers
- The Rise of the Digital Opinion Leader in Post-COVID Medical Affairs
- The Role of Medical Affairs in Combating Misinformation
- To Catch a Predator: Best Practices for Uncovering Predatory Journals and Conferences
- Top KPIs for Measuring Medical Affairs Success in 2022
- Tracking Relationships: Understanding KPIs That Measure KOL Engagement
- Trust-building in a Pandemic: Collaborative Strategies for MA teams
- Understanding Which KOLs are Key for You
- Visit us at The 15th Annual Meeting of ISMPP, National Harbor, MD
- What Happens When Medical Affairs Intersects with Politics?
- What To Look For in a Medical Affairs Customer Relationship Management Platform
- Why Life Sciences Companies Need Regular Medical Affairs Audits
- Why Medical Affairs Must Lead a Patient-Centric Approach to R&D
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