Recent Webinars

1. Qualified eSignature in Electronic Consent Systems 2/25/2026

   This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.

2. Charting The Path To First-In-Human: Strategic Readiness For Early Clinical Success 2/10/2026

   Gain a comprehensive, end-to-end perspective on the journey to first-in-human and understand how early decisions influence downstream success.

3. Embedding AI And Critical IRB Operations Data To Drive Intelligent Study Design 1/28/2026

   Explore how modern clinical trial design is being transformed by a rich array of data sources through this clear roadmap for navigating the evolving complexities of the industry.

4. CRO Selection Science: Insights From $2B+ Vendor Choices 12/15/2025

   Discover how data-driven strategies and structured RFPs can simplify CRO selection, improve transparency, and ensure the right operational fit. Learn practical steps to make smarter vendor decisions.

5. Should Sponsors Provide Source Document Templates? 12/9/2025

   Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.

6. EU GMP Annex 11: Compliance Strategy And Digital Solutions 11/18/2025

   Explore how EU GMP Annex 11 revisions could reshape global pharmaceutical compliance, as well as strategies for navigating implementation challenges and building future-ready validation programs.

7. Rethinking Effectiveness: Balancing Tradeoffs In An Era Of Disruption 11/12/2025

   In an era defined by rapid disruption and technological advancement, clinical operations leaders are under increasing pressure to enhance effectiveness while managing complex strategic trade-offs.

8. How To Select The Right Bioanalysis CRO For Your Program 11/3/2025

   The right bioanalysis CRO accelerates progress, while the wrong one can derail outcomes. When every provider claims speed and credibility, how do you confidently choose the right partner?

9. Unlock Peak Performance: AI-Powered Study Start-Up And Execution 10/14/2025

   In part two of our webinar series, speakers delve into how artificial intelligence is reshaping every stage of the clinical trial journey — from designing smarter, more feasible protocols to streamlining study start-up and execution.

10. From First-In-Human To Proof-Of-Concept — Quicker, Smarter, Streamlined 10/14/2025

    Explore examples of smarter SAD/MAD trial designs including multi-part and hybrid protocols, regulatory foresight, recruitment considerations, and operational strategies that keep programs moving.