Technology & Regulatory Affairs
AdvaMed advocates and works for a consistent, predictable, and transparent regulatory system.
Efficient and predictable regulatory processes are essential to fostering innovation and ensuring patients have timely access to safe and effective medical devices and diagnostics. AdvaMed’s Technology and Regulatory Affairs department works with the U.S. Food and Drug Administration to ensure that regulatory processes are reasonable and predictable and result in science-based decisions.
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AdvaMed members receive full access to our library of medtech resources. Become a member to receive this and countless other benefits.