Breakfast seminare: EU Medical Device Regulation and quality management systems

When: 30 January, 08.00-08.45

Where: Innovation Hub, Dag Hammarskjölds väg 38

Host: PlantVision


The medical device industry is currently preparing to go live with the medical device regulation (MDR), which will be fully applicable in May 2020.
Do you work in a start-up company, a company that brings new medical device products to market, or a medical device company that did not need a QMS according to MDD (medical device directive)?

This seminar will help you understand what you need to implement in order to be compliant with MDR and the additional challenges to come.

Coffee and sandwich will be served.

Note, the seminar will be held in Swedish, with written materials in English.



Nina Englund. Event coordinator. “My goal is that our partners and members get the very best experience when they meet and network at Uppsala BIO’s events.”

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