SCAR (Supplier Corrective Action Request) System
Automating the SCAR process with supplier corrective action request software effectively extends the corrective and preventive action (CAPA) compliance process to suppliers, streamlining all tasks related to a life science organization's SCAR process.
For life sciences organizations, accountability is a critical part of quality management and FDA compliance. In the view of regulatory agencies, it is an organization's responsibility to maintain and qualify its partners. In highly regulated life science environments, ensuring that suppliers maintain an acceptable level of quality and regulatory compliance can be a daunting task. MasterControl’s Supplier Corrective Action Request (SCAR)™ software system automates the SCAR process to reduce audit time, improve product quality and safety, and ensure regulatory compliance.
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