Description

MDMA's 2026 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. Attendees also are eligible to receive up to 6 credits towards RAC re-certification upon completion.

For more information and to register, CLICK HERE. 

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