* 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

Qualcy QMS

Qualcy QMS