Tools & Templates

Guide to Effective Medical Device Pre-Sub Meetings

MedTech
No items found.
Compliance & Regulatory: MedTech

Pre-Submissions(Pre-Subs) are a part of the FDA Q-Sub program, used to help gain FDA feedback before a regulatory submission. This resource provides tips on when you should use a Pre-Sub, what to expect from the FDA, and how to prepare for a meeting with the FDA.

Sign up below to access this Free resource!