On-Demand Webinars

  1. The Strategic And Scientific Imperative For Prospectively Generated Real-World Evidence 11/7/2022

    This webinar will explore the RWE/RWD landscape and focus on those situations in which a prospective observational study or registry presents a more optimal solution.

  2. Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF 4/17/2023

    Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.

  3. Digging Through The Hype: Can AI/ML Assist Clinical Development? 11/14/2024

    AI has great potential to enhance the efforts of your team members by accelerating data interactions. Watch this webinar and discover how AI can improve clinical trial outcomes and data management.

  4. Applying RWD: Use Cases And FDA Guidance 9/17/2024

    This presentation delves into pragmatic approaches for clinical evidence generation and regulatory acceptance. It examines recent FDA draft guidance on integrating RWD/RWE in medical device studies.

  5. Adopting Vault CDMS Accomplishments And Lessons Learned 8/31/2022

    GSK leveraged an agile approach and modern ways of working to help shorten their EDC build times. Learn how they reduced EDC build and UAT times by 50% and had all new studies built within Vault CDMS in 18 months.

  6. Improving Supply Chain: Accountability, Sustainability, Optimization

    Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.

  7. Accelerating Clinical Trials Through Streamlined Confidential Disclosure Agreements 2/9/2026

    In this presentation, Dr. Christine Senn addresses the persistent challenge of study startup delays by focusing on a primary legal hurdle: the Confidential Disclosure Agreement (CDA).

  8. Vital Sign Monitoring Using Wearable PPG Technology 11/20/2024

    Explore the latest advancements in photoplethysmography (PPG) technology and discover how innovative cardiac metrics can enhance your research by joining the Q&A session with industry experts.

  9. Practical ICH E6(R3) Oversight For Your Centralized Monitoring Strategy 3/17/2026

    Bridge the gap between fragmented data and ICH E6(R3) compliance. Learn to use unified data signals to catch consent errors and enrollment delays before they trigger audit findings.

  10. Tailoring IRT/RTSM Solutions To Overcome Challenges 12/12/2024

    Learn how RTSM can be tailored to meet precision medicine’s unique challenges of expiry, visit & personalized shipment management.