Manage the Complete Life-Cycle of the Change and Get Insights
Compliant with FDA, GMP/ GAMP, ISO 9001, and 21 CFR Part 11. Automate the process of qualifying and tracking approved and prospective suppliers based on your standard operating procedures. Monitor all vendors and keep records of all related information, including contracts, CAPA, supplier corrective actions (SCAR), ratings, engagement, and compliance. Group all of the supplier-related documents and relevant information, and bring the right people together at the right time to perform supplier-related tasks. Assure compliance and completion of needed certificates and qualification details and link to the contract management apps that are part of the PERFEQTA QMS for a more holistic approach to quality management.
(...Not Weeks, Not Months.)
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