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29 January 2018

QUNIQUE Offers MSDAP Training Programme

Are you a medical device manufacturer selling class II, III or IV medical devices in Canada?

As of January 2019, you will need an Medical Device Service Audit (MDSAP) certificate to be able to license and sell your devices in Canada.

Are you interested to know more about MDSAP, its requirements, its challenges, and tips and tricks on how to get ready for an MDSAP certification audit?

QUNIQUE is offering an MDSAP programme that provides practical training for medical device manufacturers on 21 March 2018.

The training package includes:

  • Training documents in PDF and paper
  • Training certificates
  • QUNIQUE checklists on USB stock

Contact QUNIQUE directly to reserve your seat for our training in Zurich, Switzerland.

The MDSAP Medical Device Single Audit Programme Practical Training for Medical Device Manufacturers is taking place on 21 March. 
QUNIQUE presents its seminar and workshop 'Medical Device Regulation (MDR) Performing Successful Clinical Evaluation', which will take place on the 11 January 2018 in Zurich...
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