MDCG guidance
MDCG 2019-7: Guidance on article 15 of the medical device regulation (MDR) and in vitro diagnostic device regulation (IVDR) on a ‘ person responsible for regulatory compliance ’ (PRRC)
MDCG guidance · Other topics · June 2019
Key facts
| Reference | MDCG 2019-7 |
|---|---|
| Title | Guidance on article 15 of the medical device regulation (MDR) and in vitro diagnostic device regulation (IVDR) on a ‘ person responsible for regulatory compliance ’ (PRRC) |
| Topic | Other topics |
| Published | June 2019 |
| Document | health.ec.europa.eu |
At a glance
- Yes Full text searchable in Orca1
- MDCG 2019-7 (June 2019) 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.