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SEMINAR “Regulatory.Affairs: Clinical Studies”


SEMINAR "Regulatory.Affairs: Clinical Studies"


Get prepared for the regulations of the MDR, which will apply from May 26, 2021


When: January 28, 2021 I 2.00 p.m. - 5.00 p.m.

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The new MDR leads to a change in the classification of medical products or software solutions. As a result, clinical trials may become necessary for the approval for a new medical device product or software solution

This seminar provides information, experience reports and concrete assistance on this topic. Take the opportunity to discuss with experts and to go through the individual steps of a clinical study.


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