CAPA Management Software

Generics Drug and API Manufacturers are required to create Corrective Actions/Preventative Actions (CAPAs) on the basis of client feedback, audits, complaints, deviations, or inspections. The QUMAS Quality Management Solution will ensure that corrective action plans are aligned with the source of the issue, removing the need for duplication of effort. Automated forms, business rules and a dynamic workflow engine make up the basis of the QUMAS CAPA Management Solution process, allowing for a corrective action plan to be created and executed on. Full audit trail and electronic signature functionality ensures compliance with 21 CFR Parts 210-211, 820, and 606 and EU Annex 11 requirements. This includes data integrity, traceability, data security and electronic signatures. The system allows you to automate routine operations and enhance efficiency. QUMAS preventative action software is designed to enable you to track and action CAPA deviations across multiple plants. The user-friendly interface allows you to create effective CAPA process controls.

Watch this webinar to learn about Best Practice Deviation, CAPA, and Change Control with BIOVIA QMS

- Improve Quality Control across the organization on a local and global basis
- Help to resolve Deviations and CAPAs faster
- Reduce costly product recalls
- Reporting by product in dashboard format to review efficiencies and identify process improvement opportunities
- Reduce the cost of manufacturing Generic Drugs
- Manage change control efficiently for cost reductions
- Spend less time on audits, including Agency, Vendor, Client and Internal Audits
- Respond quickly to audit findings
- Gain greater Control over your Supply Chain

Alternatively, check out this CAPA Process Package from the QUMAS Packaged Solutions, which offers an off-the-shelf approach to CAPA Management.