Inadequate CAPA processes are still the number one reason for FDA 483s.
With the FDA issuing numerous CAPA-related 483s daily, the warning signs are there.
Watch this overview video to learn
how to prevent FDA 483s with integrated nonconformance and CAPA management.
You'll learn how Pilgrim SmartSolve® supports your compliance efforts by:
Watch this overview video to learn more. »