Webinars

1. Translating R3 Data Governance And Oversight Into Practice 7/18/2026

   Learn how to translate ICH E6(R3) into practice with actionable strategies for proactive risk management, robust data governance, and earlier deviation detection.

2. Where The Data Starts: Rebuilding Sponsor-Site Alignment On Source 7/18/2026

   In this candid discussion, we cover the disconnect between sponsor-designed data systems and the way source data is actually created, managed, and verified at the site.

3. From Friction To Partnership: What It Really Takes To Become The Sponsor of Choice 7/17/2026

   Sponsors depend on sites to recruit patients, execute protocols, and collect high-quality data. In this candid panel discussion, we explore what makes sites want to work with a sponsor.

4. The Secret Sauce Behind High-Enrolling PIs 7/16/2026

   The real challenge with enrollment often comes at the screening stage, where PI prioritization, site bandwidth, and sponsor support guide how many patients actually make it onto a study.

5. From Chaos To Clarity: A Founder's View From 30 Years In Drug Development 7/16/2026

   Same workflows, higher stakes. A 30-year drug development veteran reveals how outdated sample handling puts trial outcomes at risk and what sponsors can do about it.

6. Challenges To Making Go/No-Go Decisions In Clinical Trials 7/16/2026

   In drug development, a go/no-go decision can be a high-stakes trade-off between speed and certainty. Delve into the real-world operational and strategic hurdles to making those decisions.

7. Out Of The Shadows: How Patient Advocacy Groups Are Rewriting The Clinical Trial Playbook 7/16/2026

   This panel discussion shines a light on how patient advocacy groups are rewriting the playbook on patient recruitment, education, feasibility, and real-world study support across rare diseases.