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EMA establish advisory portal for high-risk medical devicesThe European Medicines Agency (EMA), in collaboration with the European Commission (EC), has established a standard procedure for manufacturers of certain high-risk medical devices to request ...
The European Medicines Agency (EMA) said Monday it has established a way for manufacturers of certain high-risk medical devices to request scientific advice. Manufacturers of class III devices and ...
EMA, in close collaboration with the European Commission, has established a standard procedure for manufacturers of certain high-risk medical devices to request scientific advice on their intended ...
Femasys (FEMY) announces Conformite Europeene mark certification under European Union Medical Device Regulation as the first regulatory ...
The efficiency of the approval process ... are successful, the EMA plans to extend systematic monitoring into 2025 to maintain improvements. The 5th Medical Device Software Development Summit ...
A false claim is circulating online that the European Medicines Agency (EMA) has acknowledged that mRNA vaccines have not ...
The Montreal-based C3i Center obtained regulatory approval from the European Medicine Agency (EMA) to produce cell therapy therapies for the European market. The company obtained a certificate of ...
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