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FDA's 21 CFR Part 11 Add-On Inspections
Recorded WebinarNew
Regulatory & ComplianceCertificate

FDA's 21 CFR Part 11 Add-On Inspections

Navigate FDA's increased scrutiny of electronic records and software validation — implement effective 21 CFR Part 11 V&V strategies aligned with GAMP, ISO 14971, and real-world inspection expectations.

John E. LincolnJohn E. Lincoln
1.5 hours
4.8
$350.00
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