30 Jan. 2020, 08.00-08.45
Hubben, Dag Hammarskjölds väg 38 in Uppsala Science Park

(in collaboration with Uppsala BIO)
REGISTER HERE

EU Medical Device Regulation and quality management systems

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.

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

REGISTER HERE

The seminar is free of charge

Upcoming events in Uppsala…

2019-12-10 | Breakfast seminar: How will MDR impact your QMS? | Read more »

2020-01-30 | Breakfast seminar: Introducing a QMS for medical devices according to MDR | Read more »

2020-02-05 | Training course: Kvalitetssystem för medicinteknik, ISO 13485 och MDR – en introduktion | Read more »

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