MedTech Europe has updated its Code of Ethical Business Practice considering the evolution in standards since it last revised the document in 2015. The updated text features additional information on ...
Notified body (NB) availability and readiness for implementation of the EU’s medical device and in vitro diagnostic regulations (MDR/IVDR) stand out among “burning points” in need of authorities’ ...
The U.S. and the EU have signed off on a trade deal, which makes some important provisions for generic pharmaceuticals. However, Medtech Europe said in an Aug. 21 statement that it is concerned about ...
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