Event Catalog
Browse 71 professional development events
2 results
Recorded WebinarNew
Regulatory & ComplianceCertificate
IQ, OQ, PQ in the Verification and Validation Process
Develop a Master Validation Plan and defensible IQ, OQ, PQ protocols aligned with FDA cGMP, ICH Q9, ISO 13485, and ISO 14971 risk management standards.
1.5 hours
4.8
$350.00
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.
1.5 hours
4.8
$350.00