DMF Workshop: GDUFA III Enhancements and Structured Data Submissions – Session 3
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DMF Workshop: GDUFA III Enhancements and Structured Data Submissions – Session 2
24:28
Introduction to the Drug Master File (DMF) Review Process
22:08
Timeline for the Drug Master Review Process
17:02
CDER BIMO: Electronic Submission Requirements for New Drug and Biologic Licensing Applications
11:19
GDUFA III MCRM External Training Presentation final
1:42:25
FDA Clinical Investigator Training Course (CITC) 2024 – Day One – Session Two
2:14:51
FDA Clinical Investigator Training Course (CITC) 2024 – Day One – Session One
41:59