On-Demand Webinars

1. Technology Overload: Addressing Site Challenges Of Digital Trials 5/23/2024

   Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.

2. 3 Ways To Unlock The Value Of Real-World Evidence 12/13/2022

   Tune in as Castor’s Director of Solutions Consulting Kristen Harnack illustrates how a modular approach to clinical technology can help you conduct an RWE study.

3. Accelerating Rare Disease Drug Development With Wearable DHTs 12/8/2023

   Watch as experts from ActiGraph, Bellerophon Therapeutics, and IQVIA come together to explore the obstacles and potential breakthroughs in rare disease research.

4. FDA's Vision On PRO Collection For RWE 9/24/2024

   In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies, particularly in light of FDA expectations.

5. Effortless Hybrid Consent 2/22/2022

   Watch this webinar to see the latest eConsent workflow from recruitment, to pre-screening, to remote consent.

6. IRT And Direct-To-Patient Trials 1/12/2022

   Want to know more about the growth and expansion of IRT in the decentralized trial space? Witness how IRT is being used to support direct-to-patient delivery in this hybrid trial case study.

7. The eTMF As A Regulatory Standard 6/1/2023

   Discover essential insights on maintaining a high-quality Trial Master File (TMF) in a discussion about ICH GCP Essential Documents and the different regulations that apply to the TMF.

8. Advanced Features Of Castor EDC For Study Admins 1/27/2022

   During this webinar, learn tips and tricks on how to implement some of the advanced features in Castor EDC.

9. 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.

10. Reducing Macroeconomic Pressures On Clinical Trial Supply: Session 2 4/28/2023

    Join IRT industry veteran and drug supply expert Stefan Dürr for a discussion about how to reduce the impact of both traditional and emerging macroeconomic pressures on clinical trial supply.