Dear David, to become the qmsWrapper Consultant you need to be able to provide Medical Device companies with advice on how they should work in a regulated industry and guidance on how they should prepare their FDA and CE clearance submissions. To check our Partner program, please follow this link https://www.qmswrapper.com/partner-program
VALIDATED Medical QMS System purpose built to facilitate compliance with standards ISO 13485, ISO 14971, 21 CFR part 11, ISO 9001 and regulations enacted by the FDA. Very complete including: Document-
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