Regulatory / Research
15 videos • 12 views • by Cesiley Trevino
1
Registering and Reporting Results to ClinicalTrials.gov
NIH Grants
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2
Navigating the Expanding Regulations of ClinicalTrials.gov Registration and Results Reporting
Advarra
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3
An Introduction to FDA's Regulation of Medical Devices
U.S. Food and Drug Administration
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4
Learn About ClinicalTrials.gov Modernization and How to Provide Input – Mar. 6, 2020
U.S. Food and Drug Administration
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5
Common CMC (Quality) Issues and How to Avoid Them Part I (12of16) Generic Drugs Forum
U.S. Food and Drug Administration
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6
Generic Combination Products: Assessment and Regulatory Update (14of16) GDF 2020
U.S. Food and Drug Administration
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7
Still submitting paper to CDER? Send electronically with CDER’s NextGen Portal instead!
U.S. Food and Drug Administration
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8
FDA Adverse Event Reporting System (FAERS) Overview - Pharmacovigilance 2020
U.S. Food and Drug Administration
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9
Combination Products: Reporting Device Information and Malfunctions - Pharmacovigilance 2020
U.S. Food and Drug Administration
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10
Digital IND Safety Reporting - Pharmacovigilance 2020
U.S. Food and Drug Administration
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11
Pharmaceutical Quality Policies: What You Need to Know (10/15) Global Quality
U.S. Food and Drug Administration
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12
CDER Export Certificate Program - REdI 2020
U.S. Food and Drug Administration
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13
Cannabis Clinical Research: Drug Master Files (DMFs) & Quality Considerations
U.S. Food and Drug Administration
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14
FDA Announces Quality Management Maturity Programs
U.S. Food and Drug Administration
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15
The Unicorn Princess (Part 1) (Horse Game)
TSM Channel
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