* Qualcy Audit Management Software has been designed for Bio-Medical companies (including Biotech, Pharma and Medical Device) to manage QMS records for ISO13485 and FDA requirements. ?pricing_options=%5B2%5D&users=%5B64%5D&platform=%5B1%5D&sortOrder=sponsored Export category-list.sh category-slug-list.txt Designed for meeting the requirements for 21 CFR Part 820 ?pricing_options=%5B2%5D&users=%5B64%5D&platform=%5B1%5D&sortOrder=sponsored Export category-list.sh category-slug-list.txt Has built in features for E-sign, audit trails and complies with 21 CFR part 11 requirements. This software helps manage the records for Audit Plan, Audit Reports, NC Management and corrective Actions.

Qualcy QMS