10 Dec. 2019, 08.00–08.45
Conextion, Uppsala Business Park, Rapsgatan 7, Uppsala
(in collaboration with Uppsala BIO)

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. Even if you have a product certificate allowing you to sell your products under an existing MDD (medical device directive) certificate – the new requirements on QMS will be applicable from day one.

This seminar is aimed at those already working with a QMS in accordance with MDD and want to know what additional requirements MDR will place on their QMS.

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


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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