Compliance Digital Courses

Webinar Recording: Mastering FDA Inspection Readiness — Key Trends and Strategies for Drug and Device Compliance in 2025

Category
What You’ll Learn:
  • A refresher on FDA inspection fundamentals
  • Current trends and expectations for modern-day inspections
  • Practical steps to foster smooth inspections and favorable outcomes
  • Regulatory focus areas for drug and device inspections conducted by CDER, CBER, and CDRH, both domestic and international
  • Expert answers to common inspection-related questions

Description

Gain expert insights into how to effectively prepare for and navigate FDA inspections in 2025. This on-demand recording features a distinguished panel of former FDA officials and senior global quality and compliance leaders from top FDA-regulated companies. Together, they explore key regulatory trends, common inspection pitfalls, and actionable strategies to help your organization stay audit-ready in today’s complex compliance landscape.
Whether you’re overseeing compliance for a pharmaceutical, biopharmaceutical, or medical device company—or working with a CRO, IRB, or research institution—this session delivers timely, real-world guidance you can immediately apply to strengthen your inspection readiness.
Who Should Watch:
  • Supplier Quality Managers, Directors, and Engineers
  • VP/Director of Supply Chain
  • VP/Director of Procurement & Chief Procurement Officer
  • R&D Leaders and Heads of Supply Chain
  • Quality Systems Managers, Directors, and VPs
  • Chief Quality Officers and Chief Operating Officers