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Document 32022R0944
EURL tasks and criteria
Commission Implementing Regulation (EU) 2022/944 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the tasks of and criteria for European Union reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)
- Legal basis:
- 32017R0746 - A100P8PTA)
- EuroVoc thesaurus:
- health policy; single market; rules of procedure; EU reference laboratory; research body; medical device; testing; international standard; sampling; professional qualifications; operation of the Institutions; application of EU law
-
- Documents:
- Ares(2021)7122928 (Draft implementing regulation)
- Legal basis:
- 32017R0746 - A100P8PTA)
- Leading service:
- Directorate-General for Health and Food Safety
- Committee:
- Committee on Medical Devices
- Check the status of this initiative on the Better Regulation Portal
-
- Consultation type:
- Stakeholder feedback
- Consultation duration (weeks):
- 4
-
- Documents:
- C/2022/4311 final (Implementing regulation)
- Leading service:
- Directorate-General for Health and Food Safety
-
- Documents:
- 32022R0944 (Implementing regulation)
- Date of publication:
- 20/06/2022