FDA's Center for Devices and Radiological Health has provided a set of resources including videos and presentations on how to navigate the many aspects of medical device product regulations. The modules are broken into these sections:
- Registration and Listing
- How to Study and Market Your Device
- Postmarket Activities
- Unique Device Identification (UDI) System
- Specialty Technical Topics
- Radiation-Emitting Products
- In Vitro Diagnostics (IVD)
- Industry Basics Workshop Series
There is lots of good information here and new information is added weekly. We'll continue to update StartupFDA with highlights and summaries.