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)
Basic information
Dates Date of document:
  • June 17, 2022
Date of publication:
  • June 20, 2022
Date of effect:
  • July 10, 2022
    • Entry into force - Date pub. +20 See Art 19
Modified by
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Research body
  • Application of EU law
  • International standard
  • Medical devices
  • Sampling
  • Public health
  • Protection of health and safety
  • Rules of procedure
  • Internal market - Principles
  • Professional qualifications
  • Medical device
  • EU reference laboratory
  • Operation of the Institutions
  • Testing