On-Demand Webinars

31. RTSM Considerations For Master Protocol Oncology Studies 1/20/2022

    This webinar discusses the types of master protocols and how configurable, modern RTSM systems enable fast and seamless mid-study changes to help you efficiently run your master protocol study.

32. Building One Home for Sites 7/23/2024

    Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.

33. Key Considerations For A Direct-to-Patient Clinical Trial 1/20/2022

    This webinar explores important considerations for developing a Direct-to-Patient strategy and the RTSM features needed to support its execution.

34. Bridging The Gap: EHR To EDC Integration In Clinical Trials 9/9/2025

    This distinguished panel of industry experts shares an engaging and honest discussion about the current state and future potential of EHR-to-EDC integration.

35. CDISC TMF Interchange Takeaways 10/16/2023

    Follow along as experts discuss reference models for Trial Master Files in clinical studies at the Clinical Data Interchange Standards Consortium's 2023 U.S. Interchange.

36. Top 10 Questions For Selecting The Best eTMF System 4/11/2022

    An eTMF system can help Clinical Operations professionals manage the deluge of documents and data, but what capabilities are right for your situation? What is the best way to make the move to a modern eTMF from paper, spreadsheet trackers, or legacy tech to a new eTMF? Hear answers to these questions and more from a fellow Clinical Operations leader with experience in making the transition to an eTMF built for today's research ecosystems.

37. Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials 6/24/2024

    Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.

38. Mitigating Risk And Complexity In Cell & Gene Therapy Trials With IRT 8/19/2025

    CGT pioneers require supply chain partnerships that mitigate trial risk and complexity. Explore how to optimize pre-trial and pre-screening activities and reduce trial cost and risk with an IRT solution.

39. How FAIR Data Principles Power Clinical Analytics Success 11/8/2023

    Explore key challenges in accessing and preparing analytics-ready clinical data, how FAIR guiding principles can help maximize the value of clinical trial data, and the impact of innovative analytics.

40. The Role Data Quality Plays In Getting Your Product To Market 10/9/2024

    Discover how maintaining strong data integrity can transform your clinical trials and strategies you can use to optimize trial builds and streamline data collection processes, ultimately leading to faster approvals.