Medical Devices / In Vitro Diagnostics

Let the AMS  Medical Device Expert group
help you generate solutions:

 

Get premarket or postmarket phase aid for:

  • Classification
  • Regulatory tasks
  • Planning and conduct of clinical investigations / clinical performance studies around your product
  • Medical Device Vigilance

Talk or write to us:

 
AMS  also supports you in preparing HTA documents for benefit assessments of medical devices.

• 2022 – AMS are CTR- and MDR ready • 2022 – New unique AMS-ePRO® features launched • 2022 – Real-World Evidence focus in AMS Late-Stage Research • 2022 – AMS expanded its global reach • 2021 – DIGA dossier submission pioneer •

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