etmf master product release

Anju Introduces eTMF Master for Electronic Trial Master File Management

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Cloud-Based, Collaborative Solution Allows Real-Time Management of Clinical Trial Content by Sponsors, CROs and Sites   FORT LAUDERDALE, FL, June 20, 2022 (PRNewswire) –Anju today announced the introduction of eTMF Master, a new cloud-based electronic trial master file software product. The solution facilitates collaboration between sponsors, CROs and sites to efficiently and securely manage clinical […]

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etmf digital solution

Why an eTMF? It’s Time for a Specialized Digital Solution

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Clinical trials generate reams of documents. Many of these documents are produced for specific purposes or audiences. Many are subject to specific requirements that govern everything from the document’s format to the environment in which the document is produced. As documents and their requirements proliferate, so does the burden on clinical trial and medical affairs […]

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Anju CEO Laurence Birch on Price of Business Show

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Recently Kevin Price, host of the nationally syndicated Price of Business radio show, interviewed Anju’s CEO Laurence Birch. The Price of Business is one of the longest running shows of its kind in the country and is in markets coast to coast. The host, Kevin Price, is a multi-award winning author, broadcast journalist, and syndicated columnist. […]

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Data Analysis on Research for Multiple Sclerosis Day

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Multiple Sclerosis (MS) is one of the most common diseases of the central nervous system affecting 2.8 million people around the world (Cotsapas et al., 2018). Today, on World Multiple Sclerosis Day, let’s discuss the current clinical research landscape, latest advancements, and more. Multiple Sclerosis (MS) is a potentially progressive, autoimmune-mediated neurodegenerative disease of the central nervous system characterized by […]

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international clinical trials

Understanding Cross-Border Enrollment for International Clinical Trials

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International clinical trials offer a number of opportunities. Work on rare diseases becomes more feasible when patients can be drawn from a larger population. Clinical trial teams can collaborate internationally, providing more effective care and pursuing more complete results. Yet enrolling patients in clinical trials across international borders is not easy. Cross-border trial enrollment comes […]

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Latest Clinical Data

Chronic Obstructive Pulmonary Disease: Latest Clinical Data

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Interested in the current clinical landscape on COPD? Read on for an overview on the latest clinical research based on data analysis from TA Scan. Social impact Chronic Obstructive Pulmonary Disease (COPD) is now one of the top three causes of death worldwide and 80% of these deaths occur in low- and middle-income countries. More than 3 million people died of […]

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reducing patient burden

Lightening the Load: Reducing Patient Burden in Clinical Trials

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The clinical trials industry is under no illusion as to how difficult it is to recruit patients to studies and then to retain them throughout the trial. There are many perceived and real burdens patients bear when engaged in a clinical trial such as lost days from work for site visits, travel costs to get […]

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Anju’s Growth Strategy: CEO’s Perspective

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Source: Mergermarket | May 3, 2022 Anju Software, a clinical trials data and software provider, is on the lookout for large and small acquisitions to build its business while it pursues organic growth, according to new CEO Laurence Birch. Phoenix-based Anju, which has been wholly owned by Abry Partners since March 2019, could spend up to USD […]

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patient advocacy groups

Partnering with Patient Advocacy Groups Benefits Pharma and Patients

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Patient advocacy groups (PAGs) have been around since the 1950s and have fulfilled various roles such as providing material resources, knowledge and emotional support to those in need. They’ve also been vital conduits between pharma companies and the patients these companies are looking to recruit for clinical trials.   However, there are criticisms surrounding these relationships […]

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AI- Machine Learning

AI and Clinical Intelligence in Oncology Research

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Artificial intelligence and machine learning are poised to revolutionize many human endeavors, including cancer research. Here, AI and ML offer a number of opportunities to better understand existing data and make predictions based on vast datasets. Implementing these technologies in oncology research is not without its challenges. Yet many of these challenges are surmountable, and […]

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oct-europe

OCT Europe 2022: A Preview

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Outsourcing in Clinical Trials Europe 2022 (OCT Europe) takes place May 4 and 5 at the Hyatt Regency Barcelona Tower. This year’s OCT Europe, the 12th annual event, offers in-person and streaming events across both days. The goal is to provide practical advice and ideas for attendees, allowing them to improve their own clinical trials. […]

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machine Learning

Machine Learning and KOL Networks: The Future of Medical Affairs

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Key opinion leaders (KOLs) have played an important role in medical affairs for some time. For medical science liaisons (MSLs), a list of vital KOLs might include doctors, university professors and top researchers. To encourage the adoption of new forms of care, the positive regard of KOLs is essential. Building a strong KOL influencer network […]

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Data Analysis on Latest Clinical Research for Parkinson’s Day

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April 11 marks World Parkinson’s Day! A time to shine a light on Parkinson’s disease and empower yourself with data on the current clinical research landscape and the latest advancements. Parkinson’s disease is the second most common neurodegenerative disorder [1] affecting over 10 million people around the world [2]. Although the disease has no cure, the development of levodopa in the 1960s represents one of the most important […]

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Anju Appoints Laurence Birch as Chief Executive Officer

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Life Science and Data Science Industry Veteran Joins Anju’s Executive Suite; Sets Course for the Future Ft. Lauderdale, FL, April 11, 2022 – Anju, a leading provider of comprehensive software solutions to the life sciences industry, announced that it has appointed Laurence (Larry) Birch as its Chief Executive Officer. Larry brings more than three decades […]

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ready for scope

SCOPE Europe 2022: Don’t Miss These Events

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This year marks Cambridge Healthtech’s fourth annual Summit for Clinical Operations Executives (SCOPE Europe), scheduled for April 20 and 21, 2022 in Barcelona, Spain. SCOPE Europe is presented in a hybrid format, allowing both in-person and virtual attendees to participate, share and learn.   As in past years, SCOPE Europe seeks to connect, educate and […]

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understanding the value

Understanding the Value of Blockchain for Clinical Trial Data

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The past two years have dramatically changed the clinical trial industry. Trial sponsors and clinical research organizations have embraced remote trials and other creative solutions because of the pandemic. However, there are additional forms of technology that can drive trials forward while allowing firms to maintain regulatory compliance.   Here is how blockchain is used in […]

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virtual clinical trials

Benefits and Challenges in Virtual Clinical Trials

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It’s no secret just how much of a struggle it is to recruit patients to clinical trials, keep them enrolled until the study ends and, finally, get the trial drug approved. And that’s not to mention the huge costs associated with trials which are often unsuccessful or incomplete. It seems inevitable then that sponsors are beginning to […]

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Clinical Trial Data Privacy-Trial

Clinical Trial Data Privacy: What Trial Managers Need to Know

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Any conversation about data privacy in clinical trials requires understanding of key regulations. And with multinational trials commonplace, knowledge of global regulations is essential.   In the U.S., the Health Insurance Portability and Accountability Act (HIPAA) and Health Information Technology for Economic and Clinical Health (HITECH) are the priorities, whereas, European trials look to the […]

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Joe Alea Appointed EVP of Product Development at Anju

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Former Oracle and Clinical Ink Executive Will Lead Product Strategy and Development Ft. Lauderdale, FL, March 8, 2022 – Anju Software announced that it has appointed Joe Alea to Executive Vice President of Product Development. Joe has more than 30 years of clinical, healthcare, and data analytics experience. Anju Software is a leading provider of […]

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Working With Disparate Data Sources To Improve Your Trials

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For decades, trial research remained siloed, with findings carefully guarded against competing institutions. However, these data silos limit drug development, slowing down clinical trials and making them less effective.   Researchers are starting to share their findings on a global scale while turning to the data insights of their peers. At Anju Software we have […]

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Future of Decentralized Trials: Anju EVP’s Predictions

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Predictions can bring excitement, make you more aware, or produce a sense of call to action. Attendees at Outsourcing Clinical Trials West Coast 2022 in Burlingame, CA had the opportunity to experience one or more of those feelings while hearing from Anju Software’s EVP of Operations, Mike Keens, as he gave an update on his 2021 […]

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Can’t Miss Sessions at ACDM22

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This year’s Association for Clinical Data Management conference, ACDM22, is scheduled for March 13-15, 2022, taking place at the Sheraton Grand Hotel in Edinburgh, Scotland. The full program includes speakers, panels, workshops and debates featuring some of the top experts and specialists in clinical data management. Dozens of exhibitors and sponsors will be on hand to […]

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How Historical Data and Controls Improve Clinical Trials

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External data continues to be a valuable resource in clinical trial planning. When used strategically, this information can help researchers save money, increase the effectiveness of their studies, and speed up the trial. But where does historical data enter the clinical trial discussion? There are multiple ways to tap into both internal and external data […]

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Anju Software’s Pubstrat

Clinical Trial & Therapy Results: Anju’s Pubstrat MAX

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So much goes into successfully completing a clinical trial. The drug development, the testing and the patient care move a new treatment from an idea into a FDA-approved, marketable product. Concurrently, your medical affairs team must connect with key opinion leaders (KOLs), researchers, customers and potential patients — all of whom seek relevant, reliable, timely medical […]

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Impact of Cybersecurity and Data Privacy on Medical Affairs Teams

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The role of medical affairs teams continues to evolve as companies identify new ways to connect with healthcare providers. The COVID-19 pandemic provided multiple opportunities for medical science liaisons to prove their value and connect with HCPs and key opinion leaders (KOLs) virtually. However, the growth of MA teams and their use of digital communication also creates […]

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can't miss talks

6th European Clinical Research Conference: Presentations

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In February 2022, the European CRO Federation (EUCROF) is hosting the 6th European Conference on Clinical Research in Madrid, Spain. This is an opportunity for researchers to look back at the effects of the COVID-19 pandemic on the field while creating a plan of action moving forward.   Anju Software is a EUCROF partner, and will be exhibiting and […]

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Overcoming Accessibility Challenges in International Clinical Trials

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Clinical trials increasingly have international dimensions. Whether a drug developer wants to gain approval to distribute the medication in multiple countries or a research team wants to increase the diversity of participants, the international element makes clinical trials more complex.   While any challenge can be overcome, there are a few key international issues that limit […]

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AI and Machine Learning

How AI and Machine Learning Are Reshaping Clinical Trials

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The use of machine learning and artificial intelligence in society has been one of the most significant technological achievements of the 21st century. While basic AI systems were used in the late 20th century, the development of processes and systems that use ML and other functions has exponentially increased over the past decade. These technologies allow researchers across countless […]

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Gustave Roussy Renews TrialMaster EDC Agreement with Anju

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Gustave Roussy Renews TrialMaster EDC Agreement with Anju Software to Accelerate Complex Oncology Clinical Studies One of the World’s Top Cancer Research Hospitals Cites Five-Year Success with Clinical Data Management Platform for Supporting Range of Study Designs Ft. Lauderdale, FL & Paris, France, January 11, 2021 – Anju Software announced that Gustave Roussy, one of […]

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OCT West Coast: Utilizing Adaptive Systems to Get the Most from Decentralized Trials

Utilizing Adaptive Systems to Get the Most from Decentralized Trials How can you navigate your own challenges in this evolving clinical trial environment? Learn how harnessing technology will help your transition from traditional trials to hybrid and decentralized trials. Kim Rejndrup, Senior Vice President of Product Development at Anju Software, presented on “Utilizing Adaptive Systems […]

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Managing Multiple Sources within the Clinical Data Ecosystem

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Today’s clinical trials pull from several data sources. Researchers share data across departments and clinical research organizations (CROs), building on their existing knowledge to create new treatments and options for patients. Even within clinical trials, data comes in paper formats as well as digital recordings, and from AI-based systems. Somehow, all of this data needs […]

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the post-pandemic

The Post-Pandemic Future of Medical Information Call Centers

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The COVID-19 pandemic disrupted countless processes in the healthcare industry. Everything from clinical trial recruitment to medical affairs has had to adjust to an almost exclusively digital world. Nearly two years into the pandemic, industry leaders are starting to understand which changes will last and which processes will revert to pre-pandemic ways.   One significant […]

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clinical trial randomization

Enhancing Trial Planning with Screening and Randomization

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The foundation of a good clinical trial is planning. The steps you take before you ever distribute the first medication or treatment can lay the groundwork for easy data collection and positive patient experiences. The developmental stage in a trial can ensure the data is usable, accurate and defendable. You can present your information with […]

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Empower Medical Science Liaisons

How To Empower Medical Science Liaisons With Data, and Why You Should

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Medical science liaisons (MSLs) have several touch points across the healthcare field. They work within life sciences and biopharmaceutical companies to learn about products and their uses. They communicate with healthcare providers and key opinion leaders to understand industry trends. Then, they try to marry these two worlds.   There is an increasingly powerful tool […]

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Steve Rosenberg Joins Anju’s Board of Directors

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Life Science Technology Visionary Steve Rosenberg Joins Anju Software’s Board of Directors FORT LAUDERDALE, Fla.–(BUSINESS WIRE)–Anju Software has announced that Steve Rosenberg, an industry leader and innovator in developing and deploying patient-centric clinical trial technologies, has joined the company’s Board of Directors. Rosenberg also formerly led Oracle’s clinical software business. Rosenberg brings a real-world clinical […]

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patient trials

What Challenges Face Researchers With Direct-To-Patient Trials

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Most people and organizations are wary of change. New processes and opportunities create risks that could outweigh the benefits of deviating from the norm. But then a global pandemic grinds industry to a halt and requires innovations at speeds that were previously unheard of. This is what has occurred with direct-to-patient (DTP) clinical trials.   Even as […]

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Customer Relationship Management

Choosing a Medical Affairs CRM Platform: Key Considerations

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Medical affairs teams are increasingly using customer relationship management (CRM) platforms to manage how they engage with key opinion leaders (KOLs). These tools can help medical affairs teams sort through different opinion leaders and find experts with whom they can connect. There are multiple CRM options on the market, and the best ones will have been […]

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digital leadership

5 Strategies to Engage Digital Opinion Leaders

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The world is growing increasingly digital, and that includes the medical affairs process. Medical science liaisons (MSLs) are working with a new breed of key stakeholders called DOLs or digital opinion leaders. Some of these DOLs are influencers who transitioned their communication channels online during the COVID-19 pandemic, while others are social media natives.   […]

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Digital Opinion Leaders in Post-COVID Medical Affairs

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For the better part of a decade, key opinion leaders (KOLs) have been the primary source of influence in medical affairs. These opinion leaders are frequently published, highly sought after in their field and able to persuade others.   Along with KOLs, the internet has given rise to a new breed of healthcare influencers: digital opinion leaders […]

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Getting the Most Out of Your EDC Software

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Electronic data collection (EDC) tools have been proven to streamline clinical trials in several ways. These systems create faster data recording, which shortens trial periods, and provide better data as well. When clinical researchers present their findings and bring new treatments to market, they can feel confident that their studies are accurate and reliable.   […]

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ISMPP West 2021

ISMPP West 2021: Opportunities for Connectivity

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Are you attending the ISMPP West conference this month in Irving, CA? If so, don’t miss the opportunity to meet Anju Software Medical Affairs thought leaders Reed McLaughlin, Senior Vice President of Customer Management and Drew Dorman, Account Manager, to learn more about our medical publication offering. While you’re there connecting with them, make sure you ask […]

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How Technology is Moving Decentralized Clinical Trials Forward

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The use of decentralized clinical trials (DCTs) has become increasingly common, especially over the past 18 months. The COVID-19 pandemic made it dangerous to leave the house, particularly for patients with weakened immune systems. Since the start of the pandemic, the meaning of decentralized studies has evolved and new technologies have been introduced to accommodate trial leaders. […]

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HHS’ Proposed HIPAA

Understanding HHS’ Proposed Rule Changes to HIPAA

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In December 2020, the Department of Health and Human Services (HHS) issued a set of proposed modifications to the Health Insurance Portability and Accountability Act of 1996 (HIPAA). The goals of these changes are to ensure patient privacy, reduce regulatory burdens on the healthcare industry, and break down barriers that prevent organizations from helping vulnerable individuals.   The […]

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dia medical information 2021

Anju Discusses COVID Impact on Call Center at DIA

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Join Anju Software’s Global Customer Success Senior VP of Sales, Reed McLaughlin, and ProPharma Group’s Medical Information Supervisor, Americas, Stephanie Pruett and Medical Information Manager, Rachel Carlton at the DIA Medical Information and Communications Conference for an Anju Software-sponsored on-demand session: Pre and Current COVID Medical Information Call Center World. The thought-provoking session, held on October 14 at 12:30 […]

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Join Anju at Pharma Europe 2021: MSL Empowerment Talk

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You don’t want to miss the upcoming Pharma Europe 2021 virtual event held on October 11 – 22. This year’s theme: An industry awakened. Where pharma’s potential is unleashed. As a proud gold sponsor of the event, Anju Software will host a session titled Empower Your MSLs With the Power of Data on Tuesday, October 19 at 11:15 […]

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Anju Recognized in Gartner’s 2021 Hype Cycle

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Anju Software Recognized in 2021 Gartner® Hype Cycle™ for Life Science Research and Development & Commercial Operations Reports September 28, 2021 09:00 AM Eastern Daylight Time FT. LAUDERDALE, Fla.—(BUSINESS WIRE)—Anju Software has been named by Gartner as a sample vendor in four categories in its 2021 Hype Cycle Life Sciences Research and Development report[1] and Commercial […]

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edc decentralized trials

The Role of Electronic Data Capture in Decentralized Trials

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Decentralized clinical trials (DCTs) allow researchers to increase the number of participants and collect better data. However, DCTs on their own can’t do this. Lacking the right tools that make documenting symptoms and experiences easy imposes limits on the best trials.   In order to streamline the process and maintain data accuracy, more sponsors and […]

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Decentralized Clinical Trials: Post-COVID Future

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The use of decentralized clinical trials (DCTs) has increased significantly over the past year. Researchers were forced into this option because of hospital limits and local lockdowns created by the COVID-19 pandemic. However, as vaccine rates have increased, the use of decentralized trials have remained high. This trial method is the future. Here’s how researchers […]

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5 Ways to Improve the Security of Clinical Trial Data

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Technology and artificial intelligence are changing how sponsors and clinical research organizations (CROs) conduct their trials. Through their use, researchers can collect exponentially more data and analyze it more quickly and at deeper levels. However, for all of the benefits that Big Data and AI present, there are also risks. Digital threats exist in the […]

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Patient Privacy and Cybersecurity -Clinical Trials

Patient Privacy and Cybersecurity in Remote Trials

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Remote environments often create logistical challenges for trial developers. How can researchers ensure the data collected is accurate? How can they know if patients followed directions in administration and reporting? Alongside these questions, there are security concerns. Clinical research organizations (CROs) and sponsors need to protect the privacy of their patients and prevent their organizations […]

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Healthcare Cyberattacks and Clinical Data Management

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Ever since the first electronic health records (EHRs) were created, there have been concerns about security. Not only is patient privacy a significant issue (potentially fostering mistrust in the healthcare field if patient information is exposed) but so too is medical identity theft and theft of hospital financial records.   Clinical trial developers also aren’t […]

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Understanding Risk-Based Clinical Quality Management Technology

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Poor data can derail a clinical trial. It can prevent it from getting published and prevent key treatments from hitting the market. On the business side, poor data costs money because it means drug developers waste time and money on trials that don’t provide results.   More trial leaders, sponsors and clinical research organizations (CROs) are working […]

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Machine Readable Clinical Data

The Benefits of Standardized, Machine-Readable Clinical Data

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Technology creates more opportunities for pharmaceutical advancement. The rise of data collection tools, from the humble iPad to advanced monitoring devices, has allowed researchers to improve their data quality and analysis. However, it also makes processes more complicated.   Increased digital data collection means increased data sharing. If one medical professional uses a different set […]

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clinica oversight solutions

How to Use Clinical Oversight Solutions Effectively

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Changes in clinical technology allow development teams to add safety checks and balances throughout the trial process. Product developers who work closely with clinical research organizations (CROs) often set up their own oversight processes and best practices. However, the use of clinical oversight solutions is growing in popularity. Clinical oversight, in the context of clinical […]

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clinical data management ai

AI and ML in Clinical Data Management

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Artificial intelligence (AI) and machine learning (ML) have changed countless industries over the past decade. However, there’s a big difference between an AI tool alerting consumers to the contents of their refrigerators and machine learning systems driving the future of clinical trial development. Clinical research organizations (CROs) and sponsors have approached these tools with both […]

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Diverse Clinical Trials

Diverse Clinical Trials: A Necessity for Personalized Medicine

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There is a greater push in the world of medicine to provide personalized care, developing treatments based on the specific needs of one patient at a time. While personalized care can significantly improve patient outcomes, it provides its own set of challenges. How can a drug manufacturer standardize production? How can clinical researchers ensure the […]

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How to Measure the Effectiveness of Medical Information Distribution

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Medical affairs teams work tirelessly to disseminate important information and clinical trial developments. They want to make sure the research gets into the hands of key opinion leaders. This isn’t always an easy process. While MA teams can contact influencers and executives, they can’t always keep their attention or fully communicate the weight of the […]

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COVID-19’s Impact on Data Collection in Trials

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Even as vaccines are distributed across the country, the lingering effects of the COVID-19 pandemic remain. In the realm of clinical trials, researchers and administrators are left wondering what policies will remain in the future and what changes are here to stay.   One source of debate involves electronic clinical outcome assessment (eCOA) data collection […]

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AI & Machine Learning in Clinical Data Management

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July 1 + August 5, 2021 | Virtual While our yearly appointment with the Association for Clinical Data Management (ACDM) in Edinburgh in March has been delayed to next year, their eDigital Expert Group is organizing a virtual Lunch & Learn series this summer to satisfy our hunger for data. Artificial Intelligence and Machine Learning Tim […]

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New Proprietary Technology

TrialMaster 5.1: Anju Redefines Clinical Study Build Times

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Anju 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 Tempe, AZ, June 23, 2021 – Addressing some of the most time-consuming challenges of biopharma companies in building clinical studies and rolling out drug trials, Anju Software has […]

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How more data

How More Data Can Lead to Shorter Clinical Trials

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The global pandemic highlighted the necessity for some clinical trials and related data collection to be urgently expedited. While the COVID-19 vaccination results weren’t rushed, researchers did everything they could to navigate the challenges associated with developing clinical trials and analyzing data quickly. Of course, most clinical trials don’t have the same national support and […]

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Decentralized Clinical Trial Site

Early-Stage Decentralized Clinical Trial Site Selection: Key Factors

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Decentralized clinical trials allow researchers to connect with patients across the country and the world. In the case of treatments for rare diseases, decentralized trials can increase participation and create safer, more comfortable experiences for patients.   However, there is still a burden on clinical research organizations (CROs) and sponsors to choose ideal trial sites. […]

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DIA 2021 Global Annual Meeting

Anju at DIA 2021 Global Annual Meeting

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Medical Affairs and eClinical Technology Solutions Anju Software is proud to sponsor and speak at the DIA 2021 Global Annual Meeting. Join our presentation or visit our virtual booth to learn about the latest and greatest practices in clinical trial design and medical affairs technology in these turbulent times for healthcare. Innovation Theater: Utilizing Adaptive Technology Systems to Get […]

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Accuracy in Coding

How to Best Ensure Accuracy in Coding for Clinical Trials

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There are countless factors that contribute to the outcome of a clinical trial. Patient self-reporting relies on honest and accurate data from people outside of the medical field. Physicians can overlook issues or miss symptoms. Both parties can provide inaccurate information if the medical coding is wrong.   Medical codes are meant to standardize symptoms […]

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Key Opinion Leaders

How Medical Science Liaisons Should Engage With Key Opinion Leaders

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Medical science liaisons (MSLs) work with a variety of professionals including doctors, university professors, and other experts about treatments and medications developed through clinical trials. Buy-in from these key opinion leaders (KOLs) is critical to make sure new forms of care are noticed and used.   However, MSL engagement with KOLs is changing, especially in […]

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Electronic Data Capture- software Facilitates

How Electronic Data Capture Software Facilitates Cleaner Trial Data

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The use of electronic data capture (EDC) tools is changing how clinical trials are conducted. Digital systems have allowed for more decentralized studies, particularly when meeting in person was impossible during the COVID-19 pandemic. However, EDC systems provide value throughout the trial development and analysis processes. EDC technology plays a critical role in data cleaning and drives […]

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Maximizing Decentralized Trials with Adaptive Systems

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Decentralized clinical trials (DCTs) are changing how researchers evaluate treatments. However, these trials vary from organization to organization. Different levels of technology contribute to how decentralized a trial is, with more adaptive systems offering better flexibility.   The success of a trial isn’t based on its technology use, but the right tools can improve data […]

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Clinical Trial Technology

Anju at DIA China: Utilizing Clinical Trial Technology

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eClinical Software and Data Solutions Anju Software and our partner Tri-I Biotech are proud to sponsor the DIA China 2021 Meeting. Visit booth A16+17 in hall C3 to learn more about our adaptive eClinical software and data solutions that can help reduce your study timelines and save costs. Feng Cheng, Senior Vice President of Business Development Asia Pacific at Anju Software, and […]

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What is the Role of Synthetic Data in Early-Phase Clinical Trials?

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Artificial intelligence and machine learning are revolutionizing early-stage clinical trials. Technology has the power to speed up these trials — meaning they move to late-stage testing and to the general market faster — while also making them safer.   One way AI tools protect patients is with synthetic data, using either simulated data or obscured […]

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Global Annual Meeting

Top Events and Speakers at the DIA 2022 Global Annual Meeting

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The Drug Information Association (DIA) 2022 Global Annual Meeting takes place in Chicago, Illinois, this June 19 through 23. This year’s meeting is an in-person event as well as being available online.   At the DIA Global Annual Meeting, experts join forces to explore the challenges facing the life sciences community and those who work […]

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Medical Affairs Publication

Best Practices of Medical Affairs Publication Planning

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Medical Affairs-related scientific content publication planning takes countless people and several months of hard work to reach the point where the medical affairs team is ready to create a publication plan. Even during the publication process, MA teams need to keep stakeholders informed and work closely with researchers to ensure their data makes an impact. […]

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What Five Key Features Should a Trial Director Look for in an EDC?

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An electronic data capture (EDC) platform is an essential tool for clinical trials. EDC software systems sort, clean and present data accurately and efficiently. These systems can save time and protect the quality of the research. In many ways, they are the future of clinical research. There are many such tools on the market — and not […]

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How Medical Affairs Teams Can Improve Their Digital Communications

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Medical affairs professionals rely on doctor communication to share their latest treatment options and technology. But what happens when a doctor is too busy to meet in-person? What happens when a global pandemic eliminates the option to travel or meet safely?   MA teams have been improving their virtual communication practices for some time, and […]

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Join Anju at OCT Europe for Best Practices in Utilizing Decentralized Trials Technology

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May 5-6, 2021 | Virtual Conference Outsourcing in Clinical Trials Europe The leading clinical outsourcing and operations conference in Europe is returning: the 11th OCT Europe edition will be hosted virtually on May 5-6, 2021, and Anju Software is proud to participate as a sponsor and speaker. Join our presentation or visit our virtual booth to […]

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irms helps medical affairs

4 Ways an IRMS Helps Medical Affairs Manage and Share Insights

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What is IRMS? In the last decade, the emergence of digital information request management systems (IRMS) has helped revolutionize medical affairs. Before these tools, MA teams often relied on a customer relationship management (CRM) tool as the sole software for managing and handling inbound information requests. In some cases, teams had little more than spreadsheets […]

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4 Lessons CROs Can Take Away From the COVID-19 Vaccine Trials

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Bioethicists, pharmaceutical companies and contract research organizations (CROs) are going to study the COVID-19 vaccine trials and distribution for decades to come. The scale with which trials were launched and the speed at which they were completed was incredibly impressive. But industry leaders have already pointed out missteps and lessons for future improvement.   Clinical trial experts […]

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Anju Proudly Sponsors DIA MASC 2021 Forum

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March 22-24, 2021 | Virtual Conference Will we see you at DIA MASC this year? We sure hope so. Visit us in the exhibit area under Anju Software to check the latest news about our Medical Affairs product offerings or just to say hello to the team. Listen to our presentation on “Medical Affairs: from Support Function to […]

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How GDPR and Other Privacy Laws Impact Clinical Trial Data

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Clinical research has long been supported by important privacy regulations.   In Europe, the General Data Protection Regulation (GDPR) has become the gold standard for protecting the private lives of individuals. Several countries have passed their own laws that offer even further protections to citizens. At the same time, there is not complete overlap between […]

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COVID-19 Vaccine

COVID-19 Vaccine’s Impact on the Role of Medical Affairs

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Every day, more people receive the COVID-19 vaccine in one of the largest public health endeavors in history. In one month, America went from vaccinating 300,000 per day to vaccinating 1.45 million per day — and that figure continues to climb.   The pandemic changed how our world functions. The vaccines, and their rollout, will bring […]

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Medical Affairs Ecosystem

New Shifts In The Medical Affairs Ecosystem

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The evolution of Medical Affairs has been chronicled for a long time. Today, Medical Affairs informs pharmaceutical R&D. MA teams amplify the patient voice and can act as the voice of reason during a public health crisis.   This evolution has been a necessary response to the information-rich environments we all live and work in. Like so many other professionals […]

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COVID-19 Vaccine Development Enables CROs to Optimize Processes

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The rapid development, approval and deployment of the COVID-19 vaccine surprised people both inside and outside the medical field.   The vaccine was publicly fast-tracked, and the general public got a first-hand view of the development and approval process — something that typically does not make global headlines. While the vaccines’ accelerated development demonstrated a […]

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Collaboration Opportunities Between Regulators and Medical Affairs

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The role of the medical affairs team has grown in recent years. Medical affairs today serves as an important node in a network of healthcare professionals, patients and numerous other stakeholders.   As that network grows in size and complexity, everyone benefits from the symbiotic partnerships between regulators and MA professionals. Below is an overview of how […]

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Anju Leads Virtual Medical Content Compliance at TIPPA

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February 23-25, 2021 | Virtual Conference Medical Affairs-generated content is undergoing transformational change as digital platforms continue to evolve. Do Biopharma MA divisions understand the compliance implications? This is a key part of the new Medical Affairs experience and outdated technology platforms currently driving scientific content publishing will leave life sciences organizations vulnerable. Anju Leads […]

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PUBSTRAT MAX: Anju’s Innovative Publication Management

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PUBSTRAT MAX is the evolution of PUBSTRAT, the Industry-Leading Application for Publication Planning Now Available on AnjuSafe Platform, Life Science’s Most Advanced and Robust Content Management System TEMPE, AZ, 2/11/2021 – Anju Software announces the release of PUBSTRAT MAX, offering best-of-breed functionality designed for scientific and medical communications built on the new Anju Platform, AnjuSafe. […]

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How Big Data and AI Are Changing the Role of Medical Affairs & Pharma

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Medical affairs teams are growing in prominence in the pharmaceutical and clinical research communities. As more data is available to patients, payers, and physicians, MA teams fulfill a vital role of being a reliable conduit of information.   Indeed, the proliferation of data, the potential of big data, and the advancement of AI all present opportunities […]

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Data Protection Officers

CROs’ Guide to Data Protection Officers in Clinical Trials

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What is a Designated Provider Organization (DPO)?  A Designated Provider Organization (DPO) is an entity responsible for managing and overseeing the secure handling of patient data within healthcare settings. Their role extends to ensuring compliance with data protection laws and regulations, safeguarding sensitive information from cyber threats, and implementing measures to protect patient privacy.  As […]

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Join Anju at OCT West Coast: Decentralized Trials

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February 24-25, 2021 | Virtual Conference Link to recording Outsourcing in Clinical Trials West Coast Anju Software is proud to participate as a sponsor and speaker at the Outsourcing Clinical Trials West Coast Virtual Conference taking place on February 24-25, 2021. OCT West Coast is the leading clinical outsourcing and operations conference on the West Coast and […]

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Collaboration Opportunities

Collaboration Opportunities Between Regulators and Medical Affairs

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The role of the medical affairs team has grown in recent years. Medical affairs today serves as an important node in a network of healthcare professionals, patients and numerous other stakeholders.   As that network grows in size and complexity, everyone benefits from the symbiotic partnerships between regulators and MA professionals. Below is an overview of how […]

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Three Ways Decentralized Trials Bolster Patient Recruitment

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The COVID-19 pandemic accelerated many aspects of clinical research. Vaccines were developed and received the FDA’s green light in record time. Remote technologies were deployed to keep trials going, even when patients were no longer able to appear onsite.   It’s this second development that speaks to the possibilities that decentralized trials offer. Whether fully decentralized or […]

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Medical Affairs and Scientific Insights

Pandemic-Driven Medical Affairs and Scientific Insights Management

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Data collection and scientific and clinical insight management are an integral aspect of what medical affairs teams do. It’s also work that is becoming increasingly complex. The sheer volume of data generated each day in healthcare is overwhelming. Patient advocates, clinical researchers, HCPs — there are several fountains of knowledge from which to drink. Simply […]

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ISMPP EU Virtual Conference 2021

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Are you attending the ISMPP European Meeting this year? “Stop by” our booth to check the latest news about our product offerings or say hello to the team. The Anju team is excited to announce that in our never-ending quest to deliver best-of-breed, adaptive technologies, we will be launching a new, advanced version of PUBSTRAT […]

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The Continuing Rise of Decentralized Clinical Trials

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Technology plays an ever-growing role in clinical research. This includes everything from the adoption of electronic trial master files to the proliferation of virtual clinical trials. It’s the latter trend that holds special promise in the realm of clinical research. As more and more trials are conducted remotely, new opportunities arise. New patients can be […]

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How Do We Solve Pharma’s Data Dysfunction Conundrum?

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The COVID-19 pandemic was certainly an unforeseen event in 2020 that significantly impacted the pace of drug research and development, and new drug market launches and uptake. One of the key factors, however, that may have been responsible for mitigating that impact was data—both access to it and the ability to leverage it to inform […]

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Anju’s Rapid COVID Study Build in 10 Days with eClinical Suite

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Anju has been providing clinical trial platforms for cures in several areas faster than other options TEMPE, ARIZONA, UNITED STATES, /EINPresswire.com/Anju Software’s eClinical Suite, which can be deployed quicker than most other full function suites, is proud to have been on the front lines in the battle against COVID-19 since the beginning. At a time […]

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Data Protection in Medical Affairs: Basic Cybersecurity

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In early fall 2020, hundreds of Finnish psychiatric patients faced a profound fear: Someone had hacked into their therapy records and were trying to extort a ransom for that data.   Lily Hay Newman at WIRED covered the story in October. “The hacker or hackers running the extortion campaign have been demanding 200 euros’ worth of […]

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FDA Guidance and Clinical Trial Innovation: Who’s Setting the Pace?

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In March 2019, the FDA published a flurry of guidance documents regarding clinical trials. There was guidance for sponsors, and guidance for industry on Severely Debilitating or Life-Threatening Hematologic Disorders (SDLTHDs).   With these publications came a statement from then-FDA Commissioner Scott Gottlieb, who encouraged the industry to further embrace the innovations that facilitate decentralized clinical […]

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