Discussion Posts

Thread Subject Replies Last Post Community
EU MDR Annex 23.2(g): Is a lot number or serial number always required?
   
3 8 hours ago by Dan O'Leary
Original post by Anonymous Member 		Regulatory Open Forum
510(k) application for research purposes
   
5 yesterday by Anonymous Member
Original post by Shimon Vaknin 		Regulatory Open Forum
EU IVDR - prospective venous blood collection for analytical performance studies
   
0 yesterday by Anonymous Member Regulatory Open Forum
Can a PCCP be included as part of Special 510(k)?
   
0 yesterday by Anonymous Member Regulatory Open Forum
EU MDR - Can one Device have two System Basic UDI-DIs?
   
6 yesterday by Anonymous Member Regulatory Open Forum
Laboratory developed test (LDT) route
   
4 yesterday by Anonymous Member Regulatory Open Forum
Private label UDI
   
4 yesterday by Lulu Zhang Regulatory Open Forum
Internal audit schedule
   
2 yesterday by Richard Vincins
Original post by Anonymous Member 		Regulatory Open Forum
Umfrage zu ISO/TR 20416
   
0 yesterday by Florian Tolkmitt Regulatory Open Forum
Study Group for Medical Device Exam
   
1 2 days ago by Charmila Manivannan
Original post by Karen Underwood 		Regulatory Open Forum
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