Medical & Healthcare
MDR 745 Specialist
EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Use for Annex VIII classification, GSPR, clinical evaluation, EUDAMED, and UDI.
- Publisher / source
- borghei/Claude-Skills (found on the CSV list)
- Upstream record
- borghei/Claude-Skills
- Version
- Version 2
- Published
- Publication review
- Approved for publication
- Content fingerprint
0a82a7dc158c1bd6c8a435087d155288745372e2e7e0611290da9260f29846cd