Invitro Diagnostic Device CE Markingadmin2022-02-22T10:20:26+00:00
Invitro Diagnostic Device CE Marking (EU IVDR 2017/746)
The European Parliament and the Council adopted Regulation (EU) 2017/746 on in vitro diagnostic medical devices on 5 April 2017, repealing Directive 98/79/EC and Commission Decision 2010/227/EU.