What You Need to Know in 2024 for Global Clinical Trial Compliance

Tune in to Florence compliance expert, Sara Saunders as she examines US FDA 21 CFR Part 11 and its EU counterpart, Annex 11. Uncovering the foundational requirements for utilizing electronic records and signatures in the US and the comparable guidance provided by Annex 11 for European clinical trials.

In this webinar, you’ll gain:

• Key takeaways of 21 CFR Part 11 through a deep dive into the requirements
• Insights into how Part 11 requirements translate to those within the EMA
• Strategies for running clinical trials in compliance with both FDA and EMA requirements