Webinar: Clinical evaluation and clinical investigation of medical devices

May 25th, 8:30-9:30 CET

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. 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.


  • 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 for the webinar below 👇

When you've registered, you will get an email with your invitation and link to the webinar.

We will record the webinar. By attending, you agree that your name can be shown in the recording.

While you're waiting for the webinar, we have a video for you 👇

Farha's belief that medical devices can make lives better stems from her own experience - a sports accident that resulted in a fractured jaw. A couple of implants gave her new hope and a new purpose.

Farha Sayeed is a Regulatory Affairs consultant at SDS MedteQ.


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