New German medical device laws mean big changes afoot for industry
This article was originally published in SRA
Executive Summary
Fabienne Diekmann explains how things are changing for medtech under the new medical product legislation in Germany.
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GERMANY UP CLOSE: Changes to medtech laws signal new hurdles for industry
Last month, Germany adopted a regulation on the delivery of medical products and amending regulations concerning products. In the first article of Clinica’s new monthly series focused on the EU’s largest medtech market, Hamburg-based attorney Dr Fabienne Diekmann* discusses how manufacturers and distributors of medical devices and diagnostics serving the German market must adjust to these new legal guidelines