The European Commission has released a table on the existing language requirements for manufacturers under MDR and IVDR, compiling all national language requirements required for…
MDR and IVDR national implementation: Slovakia
The Medical Devices Regulation 2017/745 (MDR) and the In Vitro Diagnostics Devices Regulation 2017/746 (IVDR) have been implemented through Act 362/2011 in Slovakia. In this post, we…
MDR National implementation: Latvia
Latvia has implemented the Medical Devices Regulation 2017/745 (MDR) through its Medical Device Rule No 461 and the Procedures for conducting clinical investigations on medical devices for human…