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.
Ensure supplier corrective action requests and other quality events are handled to completion while creating a permanent record of activity for each supplier.
Leverage SCAR software's configurable workflows that not only put supplier corrective action request procedures into action, but also ensure the process and its results are repeatable and measurable.
Track incidence of SCARs and response time in a timely manner, and integrate with MasterControl’s broader supplier quality management framework to enforce higher vendor standards.
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MasterControl's integrated supplier solution benefits executives, quality professionals and even IT personnel.
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