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Webinar: Clinical evaluation and clinical investigation of medical devices

Whether you are a small medtech company or a large one, this webinar is a must-attend for anyone curious about how clinical studies on medical devices are conducted.

To place a medical device on the market, a clinical investigation might be needed to demonstrate safety and performance, including clinical benefits. There are several regulations and guidelines to follow, which we will cover in this webinar. 


  • Planning and conducting a clinical study
  • When is a clinical investigation needed?
  • Different types of clinical investigations and the regulatory pathway in Europe
  • Essential documents
  • Good Clinical Practice – GCP for Medical Device studies (ISO 14155:2020

The presenters will be Berit Larsson, a senior consultant in clinical development at SDS MedteQ and Johanna Apro, a senior consultant in clinical project management at SDS Life Science. 

Register here! 

Cytel Sweden
Sankt Eriksgatan 113, 3 tr
113 43 Stockholm
Stockholms stad
VAT nummer: SE7104093021


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