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Model Master Files: Advancing Modeling and Simulation in Generic Drug Development and Regulatory Submissions
Navigating Controlled Correspondences to Support Generic Drug Development
Cell Therapies and Tissue-Based Products: A Public Workshop on Generating Scientific Evidence to Facilitate Development
BsUFA III Regulatory Science Pilot Program: Progress Update
FDA Clinical Investigator Training Course (CITC) 2024
M13A: Bioequivalence for Immediate-Release Solid Oral Dosage Forms – Implementing the Final Guidance
Putting the Pieces Together: REMS Logic Model in REMS Design, Implementation, and Evaluation
Global IDMP Implementation – Getting Closer to the Goal
ICH M12 Drug-Drug Interaction Studies Final Guidance
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