Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
MDSAP is designed to harmonize Medical Device Manufactures’ Management System Certification using a Single Audit Program. As one of the first companies to be recognized as a MDSAP Auditing Organizations (AO) to audit to MDSAP, Intertek has observed the program's implementation from the beginning.
With ISO 13485:2003 and CMDCAS expiring, MDSAP with ISO 13485:2016 is the new industry standard with recognition by Australia, Brazil, Canada, Japan, and the United States. This webinar will cover the basics and important notes that Medical Device Manufacturers should know about the program including preparation, common questions, and the road ahead.
To view the webinar, please fill out the form below. If you have any questions, please feel free to reach out to firstname.lastname@example.org, or call 1-800 810 1195.