Event Catalog
Browse 71 professional development events
3 results
Recorded WebinarNew
Regulatory & ComplianceCertificate
FDA Labeling and UDI Essentials for Medical Products
Turn FDA labeling and UDI requirements into a controlled, inspection-ready system — cover 21 CFR 801, DMR linkage, misbranding risk, IFUs, and GUDID compliance.
José Mora1.5 hours
4.8
$450.00
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.
John E. Lincoln1.5 hoursJul 21, 2026
4.8
$190.00
Recorded WebinarNew
Regulatory & ComplianceCertificate
The FDA Medical Device File (DHF, DMR, DHR, Market Authorizations) and EU MDR Technical Documentation
Navigate FDA DHF, DMR, DHR, and EU MDR Technical Documentation requirements — understand the similarities, differences, and how to align global medical device documentation.
John E. Lincoln1.5 hours
4.8
$290.00