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Commission Implementing Regulation (EU) 2022/945 of 17 June 2022 laying down rules for the application of Regulation (EU) 2017/746 of the European Parliament and the Council with regard to fees that may be levied by EU reference laboratories in the field of in vitro diagnostic medical devices (Text with EEA relevance)
Publication metadata
- Published:
- Subject: application of EU law , costing , EU reference laboratory , medical device , operation of the Institutions , price formation , research body , testing
- OJ : JOL_2022_164_R_0007
- ELI : reg_impl/2022/945/oj
- CELEX : 32022R0945
- IMMC : C(2022)4047/1678009
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