Qualcy Systems Inc

Qualcy QMS Software has been helping Complex Engineering, Bio-Medical applications and Pharma companies manage Documents, Records, Assets and calibration records easily for ISO and FDA requirements. * Designed for meeting the requirements for 21 CFR Part 820 * Has built in features for E-sign, audit trails and complies with 21 CFR part 11 requirements. This software helps manage the records for Doc. change control, complaints, audits, CAPA, NC Records, Training Records and more. Our solutions include: 1- Calibration, PM and Asset Management 2- Document control and Change Management 3- Handling of Non conformance and customer complaints 4- Supplier Quality Management