The Leader in Quality and Compliance Management Software Solutions for Life Sciences

QUMAS is the leader in Compliance & Quality Management Solutions for Life Sciences, providing Electronic Document Management (SOPs, QA documents), Electronic Process Management (CAPA, Deviation, Change Control, Audit), and GxP Management. The QUMAS Regulatory Affairs solutions also deliver eCTD and Submission Management. All QUMAS Solutions deliver Collaboration capabilities as well as 21 CFR Part 11 Electronic Signatures and Audit Trails and simplify regulatory reporting.

With these solutions, QUMAS enables Pharma and Biotechs to get new products to market faster, while maintaining compliance with global regulations:

With these solutions, QUMAS enables Generics and API Manufacturers to get new products to market faster, while reducing costs and maintaining compliance with global regulations:

With these solutions, QUMAS enables Contract Organizations to get new products to market faster, while collaborating with partners and maintaining compliance with global regulations:

With these solutions, QUMAS enables Medical Device companies to get new products to market faster, while maintaining compliance with global regulations: