The Medical Device Manufacturers Association (MDMA)’s FDA Forum will be in Palo Alto, CA March 15-16, 2023.

The 2023 FDA Forum will feature senior officials from FDA and industry and focus on the key regulatory issues impacting the medical device industry.

Designed specifically for medical device regulatory professionals and executive decision makers, MDMA’s FDA Forum promises to deliver key regulatory insights and preview trends that will impact your regulatory and business strategies.

Topics will include

• CDRH Update
• Navigating 510(k), De Novo, PMA Programs
• Digital Health
• MDUFA V Implementation
• Post COVID Transition
• Best Practices for Pre-submission meetings
• Emerging Issues (Biocompatibility, Human Factors, Cyber Security & More)

Learn more and register today.

If you experience any issues, please contact Sheri DeVinney at MDMA via email at sdevinney@medicaldevices.org.