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:

 

Medical Devices bottom

• 2021 – New Literature Search tool launched • 2021 – DIGA dossier submission pioneer • 2021 – NIS-eTMF launched • 2021 – MDR readiness, AMS prepared for Medical Device Trials under new regulation • 2021 – VO (EU) 536/2014, AMS among the first 100 participants in the EMA CTIS Trainer Programme • 2021 – eSignature, AMS introduced DocuSign® • 2017 – Globally unique AMS-ePRO® features • 2016 – CRO of the year award •

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