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Munich MedTech
REGULATORY CONSULTING
An AR2-C2 GmbH Brand
Wesendonkstrasse 71
81925 München

Not sure how to start and what to expect from the CE certification process for your medical device?
Not sure if your device is correctly classified?
Do not know how to fit your device into the European reimbursement system?
Not sure what are the expectations of the Notified Bodies from your Technical File or QMS?
Looking for the authorized representative to support your CE MDR/IVDR certification?

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