FDA Risk Requirements for Your QMS Now & What’s Coming in 2025, QMSR & Beyond

Enjoy our discussion on what the current risk requirements are for the FDA and what risk requirements need to be implemented.

This free webinar addressed many of the FDA risk requirements for the following industries:

• Medical device manufacturers
• Pharma / Drug / OTC manufactures
• Combination device and drug manufactures
• Contract Manufactures

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What you’ll learn / gain during this webinar:

1. Now – What are the current risk requirements are
2. Up-and-Coming– Which risk requirements need to be implemented
3. How to KISS the FDA risk requirements, starting January 2025 and beyond

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Who should watch:

1. Company owners
2. Medical Device Manufacturing Leadership
3. Drug and Pharma Manufacturing Leadership
4. VP of Regulatory/Quality
5. Management Representatives
6. Quality Assurance Personnel
7. CAPA Administrators and Process Owners
8. Complaint Coordinators
9. Anyone involved with resolving the problem to avoid future FDA Inspection findings!

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About the Host

Markus Gee has 30+ years of industry experience in Quality System implementation & management with the ISO 9001 and ISO 13485 standards. This includes product development, validations of processes and products, etc.. Markus’s auditing experiences help him understand and convey what the FDA’s expectations and requirements are regarding risk and what you can do now to prepare.