MDCG guidance
MDCG 2022-11 - Rev.1: MDCG Position Paper: Notice to manufacturers to ensure timely compliance with MDR and IVDR requirements
MDCG guidance · Other topics · November 2023
Key facts
| Reference | MDCG 2022-11 - Rev.1 |
|---|---|
| Title | MDCG Position Paper: Notice to manufacturers to ensure timely compliance with MDR and IVDR requirements |
| Topic | Other topics |
| Published | November 2023 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2022-11 - Rev.1 (November 2023), MDCG 2022-11 (June 2022) 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.