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