What is MDSAP?
MDSAP (Medical Device Single Audit Program) is a jointly leveraged Regulatory Audit recognized by 6 countries/regulatory authorities. C.G. Laboratories utilizes this certification to assist in obtaining private label licensing for Canadian Class 2 medical devices for distribution inside Canada.

Benefits of MDSAP
Reduction of Regulatory Audits
Leverage Regulatory Resources
Facilitate marketing authorization where a QMS is a prerequisite
Promote consistency and predictability of Regulatory Programs
Minimize medical device manufacturing disruptions due to multiple
Regulatory Audits

For Additional Information contact Russell Crum
817.279.1945 Ext. 1
rcrum@cg-labs.com

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MORE ABOUT US

C.G. Labs began life in 1983 as a microbiology laboratory founded by Dr. Glenn Crum. In 1996, we relocated to Granbury, TX and expanded our services to include medical device contract manufacturing. We have grown into a multi-service company with three distinct divisions with 19,000 square feet spanning two sites.