FDA Crackdown 2025: How to Stay Compliant as Enforcement Accelerates
For all of us working in life sciences, the ripple effect of what happened in September with the FDA's recent wave of enforcement activity, driven by a new HHS directive, caught the entire industry off guard. That's why I can't wait to moderate a special one-hour webinar on November 20 at 2:00 p.m. ET in partnership with BIO.
FDA enforcement of promotional content is intensifying, and the stakes have never been higher. In just the past few weeks, the FDA has issued more Untitled Letters than in all of 2023—with major pharmaceutical companies now facing increased regulatory scrutiny.
Join us for this timely discussion featuring industry experts who will provide actionable insights on how to navigate this evolving regulatory landscape.
Key Topics We'll Cover:
- Understanding the current FDA enforcement trends and what's driving them
- Practical strategies for staying compliant in a heightened enforcement environment
- How AI technology can help ensure promotional content meets regulatory standards
- Best practices for MLR review processes
Don't miss this opportunity to hear from compliance experts and stay ahead of regulatory changes.
About SecureCHEK AI
SecureCHEK AI helps pharmaceutical and medical device companies precheck promotional content before MLR review to ensure compliance with FDA regulations.