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GERMANY UP CLOSE: Changes to medtech laws signal new hurdles for industry

This article was originally published in Clinica

  • News
  • Fabienne Diekmann

Executive Summary

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

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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