medical-explore-dqs-technology in the hospital with doctors in the background

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

First you need to register. Please use the form on this page.

After registration, you will receive an e-mail from us asking you to confirm your e-mail address.

Please note: Without confirmation, we cannot send you the link to the webinar.

After confirming your email address, we will send you the link to the webinar recording.