European Union · regulation

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)

EU law (EUR-Lex)
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Key facts
Organisation European Union
Document type regulation
Adoption date
Source EU law (EUR-Lex)