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MDSAP: One set of requirements covering 5 markets.


The Medical Device Single Audit Program (MDSAP) reduces the number of audits or inspections and the time and resources used on audit activities for medical device manufacturers.

It allows the quality management system to be audited once to satisfy the legal requirements in five markets – Australia, Brazil, Canada, Japan and the USA.

Enrolling in the MDSAP is evidence of a medical device manufacturer’s commitment to quality management systems for product quality and regulatory compliance.

Download the factsheet to learn more about MDSAP, the benefits and how LRQA can help you achieve compliance.



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