FDA-CDRH recently announced the addition of five new modules to the CDRH Learn Program website. CDRH Learn is a set of online education modules designed to provide information on medical device laws, regulation, and policies. The main page, which provides access to the modules, is http://www.fda.gov/training/cdrhlearn/default.htm
The newly added modules are:
- Unique Device Identification (UDI) System Regulatory Overview
- Global Unique Device Identification Database (GUDID) Account Request: Preparation and Process
- The GUDID Device Identifier (DI) Record
- HL7 SPL Submission Option
- Unique Device Identification (UDI) Part II, Submitting Information to GUDID