A snapshot of global medical device approvals captured during the past week in Medtech Insight's Approvals Tracker. The week of July 23 to 29 was another slow one for FDA approvals, with no new PMAs, panel-track PMA supplements, de novos, or non-US approvals.
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The US Food and Drug Administration did not approve any original PMAs or panel-track PMA supplements during the week of 23 July to 29 July.
Broad participation by EU member states in a new pilot to test a unified procedure for evaluating applications for combined drug and IVD studies shows they recognize its value, says Monique Al, vice-chair of the Clinical Trials Coordination Group.
MedTech Europe is ready to become involved and shape Europe’s Life Sciences Strategy and help drive regulatory simplification from the top to make the EU “the world’s most attractive place for life sciences by 2030.”