Regulatory Kick Start for your medical device or IVD

Clarify your individual questions about technical documentation, quality management, and the new EU regulations.

In the joint consultation, we offer you a fundamental assessment of the regulatory pathway for the approval of your medical device / in vitro diagnostic device.

For this purpose, please send us a product presentation in advance, as well as up to three specific questions that we will address during the meeting.

We look forward to exciting conversations!

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Regulatory Kick Start for the approval of your medical device or IVD:

  • 1,5 consultation hours
  • At your premises or remotely with one of our experts
  • Euro 750,- (excluding VAT) including preparatory work
  • plus travel expenses outside Vienna

Please allow approximately 4–6 weeks lead time for scheduling an appointment!

Make an appointment now