Introduction to the Medical Device Single Audit Program MDSAP
Webinar recording
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. What does that mean for your organization?
DQS offers the MDSAP service through authorizations and oversight by DQS Medizinprodukte GmbH which is a MDSAP Recognized Auditing Organization.
Please join us for a free webinar recording presented by Marc Goedecke who heads our MDSAP program at DQS MED.
The webinar at a glance:
Benefits of MDSAP certification for your company
Additional requirements beyond ISO 13485
Frequently Asked Questions and your next steps
Duration: 42:00 min
How to get to the webinar recording
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