Our Medical Affairs experts, including Reed McLaughlin, Rachel Sheldon, and Steve Anzuini, are looking forward to meeting you in booth #7. If you want to streamline your medical information and scientific communications process, book a meeting with Reed and the team, they will show you how Anju's best-in-class Medical Affairs and scientific publication management solutions can support your team and enhance their performance.
Visit booth G21 in Zhanjiang Science Hall - Floor 1 to learn how our eClinical solutions can accelerate the management and execution of your clinical trials, or book an appointment with Huiqin Yang, Manager of Business Development, China.
Join Anju Software at the Outsourcing in Clinical Trials: Medical Devices USA 2025 conference. From June 3-4 in Minneapolis, Minnesota, this event brings together MedTech leaders to explore the latest regulatory updates, trial technologies, and outsourcing strategies shaping the future of medical device research in the US and EU.
From AI regulation and post-market surveillance to clinical trial optimization, the agenda is packed with actionable insights and networking opportunities.
📌 Meet Anju’s Nate Anglin and David Kirschenbaum onsite to learn how our solutions can support your MedTech clinical operations.
- Gain a Competitive Edge: Learn how to apply clinical intelligence alongside operational insights to create precise, predictable enrollment models with our Trial Feasibility Flex module.
- Optimize Site Selection: Discover how to prioritize the best sites based on experience and capacity, while fine-tuning parameters to meet your unique trial needs.
- Plan for the Unexpected: Understand the importance of risk mitigation strategies, utilizing your CTMS alongside data strategies to protect your trial from unforeseen challenges.
- Achieving Precision in your Enrollment Modeling: Explore the importance of both internal and external intelligence to achieve precise, predictable enrollment projections
- Optimizing Site Selection: Strategies for prioritizing sites based on their experience and capacity, with the ability to fine-tune site recommendations and outputs by tailoring trial parameters
- Exploring TA Scan’s Award-Winning Feasibility Flex: A look at how this Best of Show-winning tool enables tailored trial modeling, outcome predictions, and risk mitigation.
- The Power of Data: Discover how a data-driven methodology can enhance your investigator selection process, ensuring your clinical trials are set up for success.
- Creating the Ideal Investigator Profile: Learn how to identify investigators with the right expertise for your specific clinical study, particularly in oncology, CNS, and rare diseases.
- Real-World Applications: Gain insights from practical use cases and examples of how data has been used to improve investigator selection and drive better clinical trial outcomes.
- Efficiency Boost: Discover how MA Knowledge simplifies the search for scientific content, saving time and improving productivity.
- Personalized Insights: Learn about Smart Filtering, which delivers the most relevant, customer-focused content tailored to your needs.
- Seamless Integration: See how MA Knowledge integrates with IRMS MAX for a unified, powerful platform.
- Practical Applications: Explore real-world examples of how MA Knowledge solves common Medical Affairs challenges.
- Understand the fundamental importance of Strategic Communication Plans in medical affairs and how they ensure the impactful dissemination of scientific information.
- Discover the advantages of utilizing publication management platforms for better organization, increased efficiency, compliance, and maximizing the impact of scientific communications.
- Explore the synergistic benefits of integrating Pubstrat MAX and Polarix.io, including improved collaboration and visibility, through practical case studies and examples.
- Enhance Data Integrity and Accuracy -Understand the importance of robust data integrity and how real-time data validation mechanisms can transform your clinical trials, ensuring accuracy from the start.
- Optimize Trial Builds and Data Collection – Learn how TrialMaster’s immediate feedback on input errors minimizes mistakes, while exploring strategies to expedite trial builds and optimize data collection processes for faster, more efficient trials.
- Achieve Faster Approvals – Discover best practices for quick error detection and resolution, significantly speeding up trial initiation, and positioning your product for quicker approvals by leveraging efficient trial build capabilities.
- Understand the crucial role of CRAs in trial success
- Discover strategies to optimize resources and slash timelines
- Explore game-changing features of CTMS
- Engage with industry leaders in a dynamic panel discussion
- Credibility in the Fast Lane: Discover strategies to build credibility from the outset, ensuring a robust relationship between sponsors and CROs.
- Data-Driven Differentiation: Explore the power of data in reshaping the full-service CRO sales landscape. Learn how leveraging the right data can save time, streamline processes, and provide differentiation crucial for the RFP and Bid Defense process.
- Efficiency Through Insights: Gain insights into utilizing data to project realistic timelines, manage resource limitations, and ensure the delivery of high-quality outcomes.
- how technology can assist you with country/investigator selection
- how to gain a complete view of your trials from multiple data sources
- how to design a hybrid monitoring strategy
- how to reduce study set-up time
- and how to minimize cost and disruption during mid-study protocol amendments
- How to design a hybrid study
- How to reduce study set-up time
- How to better manage mid-study protocol amendments
- How to get SDTM data out
- Integration points
- this is test
In the classic tale of the three little pigs, only one house stood strong against the big bad wolf. In clinical trials, the same principle applies: success hinges on the strength of your trial design and planning. Will your trial crumble like straw or sticks, or will it endure the test of time like a house built with bricks?
Clinical feasibility has evolved significantly, with access to robust data and intelligence tools. Yet the most successful trials blend data insights with real-world clinical expertise, ensuring precision in trial design, feasibility and enrollment. With increasingly granular patient sub-populations and global competition bringing increased challenges, it’s essential to build your trial on a foundation strong enough to withstand operational and recruitment challenges—the unexpected ‘wolves’ that threaten success.
Watch as Anju’s experts, Barbara Argibay, Vice President and General Manager, Data Solutions, Elke Ydens, Associate Director of Business Solutions, and Laura Acosta, Vice President, Product Management in the eClinical division, guide you through actionable strategies around enrollment modelling, site selection and risk mitigation, to ensure your trials are built to last.
Why You Should View this Recording:
Whether you’re a seasoned clinical operations professional or new to strategic feasibility planning, this session will equip you with the insights and tools to design trials that succeed in today’s competitive landscape. Don’t let your trial fall victim to the big bad wolf—join us and build it with bricks!
Barbara Argibay, Vice President, General Manager – Data Division at Anju, With over 15 years of experience in Data and Clinical Research, Barbara Argibay leads the Data Division at Anju, overseeing TA Scan and Data Science Solutions. Barbara’s prior experience within operations, product development, and postdoctoral research puts her at the intersection of data, analytics, insights, and strategy to support the life sciences delivering impactful results. Connect with Barbara on LinkedIn.
Elke Ydens, Associate Director of Business Solutions at Anju, Elke Ydens joined Anju’s Data Division over 5 years ago and currently holds the position of Associate Director of Business Solutions. She serves as a Subject Matter Expert for Anju’s Data Science offerings and is involved in identifying prospect/customer requirements and needs.
Elke holds a PhD in Biochemistry and Biotechnology and has almost 10 years of experience in the Life Sciences sector, including post-doctoral research positions in both academia and the pharmaceutical industry. Connect with Elke via LinkedIn.
Laura Acosta brings over 25 years of experience in life sciences software, including significant roles at Oracle Health Sciences. With academic credentials from Boston University and Tufts University in Computer Science, Laura excels in navigating the complexities of eClinical solutions. Her commitment to continuous learning and innovation has earned her recognition as a trusted leader in the field.
Access to high-quality data has revolutionized clinical feasibility, making it more robust, accurate, and efficient, and enabling evidence-based decision-making to improve trial outcomes. However, the most successful feasibility studies go beyond data alone—blending clinical intelligence with the real-world expertise of clinical teams in their disease areas.
View the webinar with Anju’s experts, Jenna Morris, Executive Director of Data Solutions, and Elke Ydens, Associate Director of Business Solutions, as they explore the power of combining internal and external data insights for precision enrollment modeling. Discover how TA Scan’s innovative Trial Feasibility Flex tool empowers teams to integrate their own insights, driving more accurate and informed projections.
In this webinar, we cover…
John Coritz, Senior Director of Customer Success at Anju, John Coritz is the Senior Director of Customer Success at TA Scan, Anju Software, boasting an impressive career spanning over 30 years in Pharma, Clinical Trials, Digital Technology, Data Analytics, and Strategic Clinical Planning.
An advocate of transparent communication, John is a firm believer in consolidating all business intelligence data sources to facilitate informed and actionable decision-making. With a wealth of experience, he stands as a seasoned professional dedicated to advancing success in the intersection of pharmaceuticals, technology, and strategic planning. Connect with John via LinkedIn.
Jenna Morris, Executive Director of Data Solutions at Anju, Jenna Morris has over 18 years of experience in data, clinical technology, and clinical research, supports the global strategy of Anju’s Data Division as a Strategic Subject Matter Expert. This role focuses on driving clinical trial efficiency through data-driven insights, advanced technologies, and strategic operational frameworks. With a commitment to optimizing clinical trial processes, the Director ensures precision and maximized outcomes for impactful research programs. Connect with Jenna via LinkedIn.
Elke Ydens, Associate Director of Business Solutions at Anju, Elke Ydens joined Anju’s Data Division over 5 years ago and currently holds the position of Associate Director of Business Solutions. She serves as a Subject Matter Expert for Anju’s Data Science offerings and is involved in identifying prospect/customer requirements and needs.
Elke holds a PhD in Biochemistry and Biotechnology and has almost 10 years of experience in the Life Sciences sector, including post-doctoral research positions in both academia and the pharmaceutical industry. Connect with Elke via LinkedIn.
In today’s highly competitive clinical research landscape, selecting the right investigators is more critical than ever. High physician turnover and growing competition have made it increasingly challenging to maintain successful clinical trial programs. Investigators play a pivotal role in patient recruitment and retention, making strategic and informed investigator selection crucial for ensuring robust study outcomes.
View Anju’s recorded webinar to explore how a data-driven approach can revolutionize your investigator selection process. By evaluating investigators based on scientific contributions, clinical experience, and proven track records, you can make informed decisions that directly impact the success of your trials.
This recording will delve into real-world examples, demonstrating how life sciences organizations can leverage data from research publications, clinical trial databases, and professional networks to identify the ideal investigator profiles for oncology, CNS, and rare disease studies.
What You’ll Learn:
Meet the Experts:
Our webinar was led by Elke Ydens and Barbara Argibay, industry veterans with extensive experience in clinical research and investigator selection. They shared their insights and guided the user through the best practices for leveraging data to improve clinical research programs.
View the Webinar
Elke Ydens, Associate Director of Business Solutions
Anju’s Data Division over 5 years ago and currently holds the position of Associate Director of Business Solutions. She serves as a Subject Matter Expert for Anju’s Data Science offerings and is involved in identifying prospect/customer requirements and needs.
Elke holds a PhD in Biochemistry and Biotechnology and has almost 10 years of experience in the Life Sciences sector, including post-doctoral research positions in both academia and the pharmaceutical industry.
Barbara Argibay, Vice President, General Manager – Data Division
With over 15 years of experience in Data and Clinical Research, Barbara Argibay leads the Data Division at Anju, overseeing TA Scan and Data Science Solutions.
Barbara’s prior experience within operations, product development, and postdoctoral research puts her at the intersection of data, analytics, insights, and strategy to support the life sciences delivering impactful results.
View this webinar recording to explore the key features of MA Knowledge, including Smart Filtering, robust search capabilities, and an intuitive dynamic workspace. Through real-world use cases, we show you how MA Knowledge solves common challenges faced by Medical Affairs teams, from curating content to delivering personalized insights. Witness how MA Knowledge empowers your field medical team with precision, efficiency, and credibility to deliver exceptional medical information tailored to their needs.
Key Takeaways
Watch the recording of John Ferguson, Steven Anzuini, and Reed McLaughlin for an engaging session focused on the release of MA Knowledge. This event is tailored to show you how MA Knowledge offers precise search capabilities, an intuitive interface, and seamless integration with your existing tools, all designed to support your team’s efficiency and effectiveness.
View the Webinar
Reed McLaughlin , Senior Vice President, Customer Management
Reed McLaughlin has spent the last 14 years developing an unparalleled rapport with clients and customers to create environments of success. As Senior Vice President of Sales, Mr. McLaughlin has been able to continually grow the business and improve Anju’s outreach and strengths. A leader in Sales and Customer Service, Reed has helped elevate Anju toward a brighter future.
John Ferguson, VP of Product Management for Medical Affairs
John Ferguson, VP of Product Management for Medical Affairs at Anju Software, boasts over 15 years of experience, holding various titles such as business analyst and director. In his role, he oversees project management and software implementation for global pharmaceutical companies, ensuring seamless integration and optimal performance. With a background in finance and an MBA from DePaul University, John’s dedication to continuous improvement drives innovation and success in the medical affairs sector.
Steven Anzuini, Senior Solution Engineer at Anju
Steven Anzuini brings over a decade of experience in the life sciences software industry, with seven years dedicated to Anju after its acquisition of OpenQ in 2017. With a BS in Communication from James Madison University, Steven draws inspiration from industry leaders like Jim Zuffiletti and actively engages with associations like ISMPP to stay updated on industry trends.
In the ever-evolving field of medical affairs, mastering Strategic Communication Plans (SCP) is crucial for ensuring impactful dissemination of scientific information. This webinar, hosted by industry experts, delves into the significance of SCPs, the role of advanced publication management platforms, and the synergistic benefits of integrating your SCP and publication management platform.
View this webinar and you will:
Anju and 9 Labs experts, Steven Anzuini, Rachel Sheldon, and Justin Erswell host an informative session designed to empower medical affairs professionals with the knowledge and tools to master strategic communication and publication management.
Check out this insightful webinar recording on the importance of data integrity and efficiency in clinical trials. Explore how Anju’s TrialMaster solution uses real-time data validation to maintain robust data integrity and streamline trial processes. Learn effective strategies to expedite trial builds, optimize data collection, and achieve faster trial approvals. This session will provide valuable knowledge for clinical researchers, trial sponsors, and industry professionals looking to navigate the complexities of clinical research with greater confidence and precision.
Key Takeaways:
Anju’s Laura Acosta, VP of product management, Caterina Cammalleri, Director of Clinical Operations, and George Naxera, VP of Business Development hosted an in-depth technical session that will provide you with advanced knowledge and cutting-edge tools to address common challenges in clinical trials. Learn how our innovative solutions can enhance data integrity, streamline trial builds, and accelerate your product’s journey to market. This webinar is your opportunity to solve critical issues, improve operational efficiency, and achieve superior research outcomes with confidence. View Recording.
Anju, On-Time Trials, and Barrington James, innovative leaders in the life sciences space, hosted a power-packed webinar designed to elevate your clinical research game. In just under 60 minutes, uncover the keys to success in sourcing, managing, and tracking clinical trials. Expert sessions feature Barrington James shedding light on the role of Clinical Research Associates (CRAs), On –Time Trials unveiling resource optimization strategies, and Anju exploring the advantages of CTMS adoption for sponsors, CROs, and associated stakeholders.
Don’t miss out—register now to view the webinar and revolutionize your approach to clinical trials!
This webinar on meeting diversity goals in clinical trials, co-hosted by Laura Acosta, Anju’s VP of Product Management, and Elke Ydens, our Associate Director of Business Solutions, explores how regulatory agencies, CROs, and industry leaders are striving to enhance accessibility to clinical trials for under served populations, aligned with the DEPICT ACT’s call for Diversity Action Plans. Discover innovative strategies and technology’s role in this pivotal mission. Watch recording here.
Our Anju hosts welcomed St. Jude Children’s Research Hospital’s Senior Manager-Clinical Research Systems from the Department of Cancer Center Administration Namratha Intha to talk about challenges with complex trials such as oncology, and how finding the right EDC solution can help you meet those challenges. Register here to view the webinar.
The right key opinion leader or KOL identification — with whom medical science liaisons (MSL) communicate and engage — can transform the effectiveness of the medical affairs and field medical teams. The MSL-KOL relationship can be crucial to successful patient outcomes.
Watch this webinar to learn how to move your MSL-KOL relationships from perfunctory to powerful. Join the featured speakers in reviewing the importance of KOL Identification and management and learn how to leverage the right technology and tools to create a quality engagement.
This webinar focuses on the various solutions needed for conducting decentralized clinical trials (DCTs)/hybrid clinical trials, including the interoperable technologies and partnerships required to provide the best patient experience.
Watch this webinar for ways to engage and retain patients and the factors to consider for implementing a successful end-to-end solution when evaluating or adopting technologies used in decentralized/hybrid clinical trials.
Watch our webinar to learn how artificial intelligence-assisted insights are helping medical affairs to measure outcomes, improve decision-making and reveal previously hidden impact insights.
During the conference Anju Senior Solutions Engineer, Medical Affairs Division, Steven Anzuini, presented a Hot Topic session titled “Managing Investigator and Internally Sponsored Publications”.
Anju Software has designed a compliant Approval Request solution within its Medical Affairs software, Pubstrat MAX. With Pubstrat MAX, anyone can easily submit a request to have their data or documents approved before sharing with internal teams or disclosing to the public. Anju’s Approval Request feature enables both internal and external stakeholders to answer a few questions, upload their document, and monitor the status of their request easily and compliantly.
Let’s talk about how a compliant request solution can help streamline your organization’s publication approval process.
On Wednesday, October 27th, Reed Mclaughlin and Kelly Malloy from Anju Software joined Donald L. Davis on the Life Science Success podcast. The discussion was centered around Reed and Kelly’s perspectives on the evolution of the Medical Affairs function, how it continues to emerge as a strategic pillar within life sciences organizations, and its critical importance to driving patient outcomes. They discussed how Anju Software medical affairs solutions like IRMS MAX and Pubstrat MAX are being leveraged to optimize work across medical affairs to increase effectiveness and leverage insights to ensure the right information is delivered to the right person at the right time.
The DIA Medical Information and Communications Conference is designed by medical information professionals for medical information professionals, building on a long series of very successful past editions. In this conference, we will leverage learnings on how to improve customers’ experience as they engage with pharma/biotech companies via various touchpoints. We will also explore when and how to successfully partner with suppliers.
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 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 PM CET, looks at how a Medical Information Call Center adapts from a pre-COVID world to service their customer base during a global pandemic.
IRMS MAX, the gold standard of Medical Information solutions, offers unsurpassed capabilities, an intuitive user experience, and the ability to deliver the right information, to the right consumer, at the right time. Anju Software is leading the charge in assisting medical information practitioners adapt in a COVID world.
You don’t want to miss this insightful on-demand session. Click here to watch.
Anju Software was a proud Gold Sponsor of the Pharma Europe meeting, formerly known as eyeforpharma Barcelona. Our Data Science Solutions Specialist Elke Ydens gave a presentation about empowering your MSLs with the power of data. You can watch the recording here.
Innovation Theater: Utilizing Adaptive Technology 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 and data will help your transition from traditional trials to hybrid and decentralized trials. Kim Rejndrup presented jointly with Laura Acosta on “Utilizing Adaptive Technology Systems to Get the Most from Decentralized Trials” in the Innovation Theater. More specifically, this presentation sharing insights on:
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 to Get the Most from Decentralized Trials”. This presentation sharing insights on:
