MDCG guidance
CAMD FAQ: CAMD MDR/IVDR Transition Subgroup: FAQ - MDR Transitional provisions
MDCG guidance · Other guidance documents · January 2018
Key facts
| Reference | CAMD FAQ |
|---|---|
| Title | CAMD MDR/IVDR Transition Subgroup: FAQ - MDR Transitional provisions |
| Topic | Other guidance documents |
| Published | January 2018 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- CAMD FAQ (January 2018) Revisions on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MDCG guidance documents
The Medical Device Coordination Group (MDCG), made up of EU member-state experts, endorses guidance on applying the Medical Devices Regulation (EU) 2017/745 and the In Vitro Diagnostic Regulation (EU) 2017/746. Each page here covers one document and all of its revisions.