IVDR
In Vitro Diagnostic Regulation (EU) 2017/746 related resources
2 resources
All Resources
FDA Guidance (106)
MDCG Guidance (69)
Clinical Investigation and Evaluation (17)
MDR (15)
White Paper (15)
New Technologies (7)
Borderline and Classification (5)
Other / Transition (5)
Post-Market Surveillance and Vigilance (4)
Notified Bodies (4)
UDI (3)
Annex XVI Products (3)
EU Regulation (2)
EUDAMED (2)
IVDR (2)
Standards (1)
Class I Devices (1)
2 resources in IVDR