Draft Commission Implementing Regulation amending Implementing Regulation (EU) 2022/1107 laying down common specifications for certain class D in vitro diagnostic medical devices in accordance with Regulation (EU) 2017/746 of the European Parliament and of the Council; (4 page(s), in English), (41 page(s), in English)

Draft amendments to the Rules for conducting clinical and clinical laboratory tests of medical devices; (75 page(s), in Russian)

Guidelines on Regulatory Reliance on the Conduct of Clinical Trials in the Philippines; (6 page(s), in English)