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The Turkish Pharmaceuticals and Medical Devices Authority recently announced that the draft amendments to the Regulation on Clinical Trials of Pharmaceuticals and Biological Products and the European Commission's Implementing Regulation Draft regarding the nonmedical product groups listed in Annex 16 of Regulation (EU) 2017/745 on medical devices are open for public consultation.
By Esin Attorney PartnershipThe Turkish Pharmaceuticals and Medical Devices Authority recently announced that the draft amendments to the Regulation on Clinical Trials of Pharmaceuticals and Biological Products and the European Commission's Implementing Regulation Draft regarding the nonmedical product groups listed in Annex 16 of Regulation (EU) 2017/745 on medical devices are open for public consultation.