Event Catalog
Browse 71 professional development events
3 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 Inspections After QMSR: What Replaces QSIT 2.0 — The New Inspection Reality
Understand the new QMSR inspection reality — what replaces QSIT, how FDA will inspect under ISO 13485 alignment, and how to manage the hybrid compliance burden of QSR + QMSR.
1.5 hours
4.8
$390.00
Live WebinarNew
Regulatory & ComplianceCertificate
Beyond Digital Batch Records: Managing FDA and EU GMP Documentation While Preserving Data Integrity
Learn how digital/electronic DHF, DMR, DHR, and EU MDR Technical Documentation improves data integrity, reduces human error, and simplifies global regulatory compliance.
1.5 hoursJul 21, 2026
4.8
$190.00