MDSAP is designed to harmonize Medical Device Manufactures’ Management System Certification using a Single Audit Program. MDSAP with ISO 13485:2016 is required if you provide medical devices into Canada and can streamline the regulatory application process for medical devices provided into Australia, Brazil, Japan, and the United States.
DQS Inc. offers the MDSAP service through authorizations and oversight by DQS Medizinprodukte GmbH which is a MDSAP Recognized Auditing Organizatoin. Please join us for a webinar presented by Marc Goedecke who heads our MDSAP program at DQS MED.
This webinar covers the benefits of MDSAP certification and highlight the additional requirements beyond ISO 13485:2016. Participants will learn tips for preparation, answers to frequently asked questions and gain an understanding of the application and audit process.
