MDCG guidance
MDCG 2021-20: Instructions for generating CIV-ID for MDR Clinical Investigations
MDCG guidance · Clinical investigation and evaluation · July 2021
Key facts
| Reference | MDCG 2021-20 |
|---|---|
| Title | Instructions for generating CIV-ID for MDR Clinical Investigations |
| Topic | Clinical investigation and evaluation |
| Published | July 2021 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2021-20 (July 2021) 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.