Tag: Form FDA 483

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Recent Related Articles to Form FDA 483

Monoclonal Antibody from Vir and GSK is 85 Percent Effective | 2021-03-11 | FDAnews

Added to Collection on: 2021-03-12 18:12:40

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Food and Drug Administration
United States Public Health Service
Health
Pharmaceutical industry
Clinical research
Clinical trials
Form FDA 483

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Roche's Actemra Missed All Key Endpoints When Paired with Remdesivir to Treat COVID-19 ...

Added to Collection on: 2021-03-12 18:12:46

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Food and Drug Administration
United States Public Health Service
Health
Pharmaceutical industry
Clinical research
Clinical trials
Form FDA 483

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FDA approves safety labeling changes for opioid pain medicines

Added to Collection on: 2023-12-15 21:11:54

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Food and Drug Administration
Foscarbidopa/foslevodopa
Form FDA 483

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Hedge Funds Watching Drug Makers - Law Street Media

Added to Collection on: 2024-02-14 20:45:33

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Food and Drug Administration
Form FDA 483
FDA Adverse Event Reporting System
Illinois Freedom of Information Act
Freedom of Information Act
Astellas Pharma
Pharmaceutical industry in China
Adverse event
Pharmaceutical industry
Adverse effect
Freedom of information laws by country
Establishment Labs
Catalent Indiana LLC

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FDA Inspection Preparedness and Compliance Seminar: Information and for Tools ...

Added to Collection on: 2024-09-02 15:34:23

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Food and Drug Administration
Quality
Inspection
Form FDA 483
FDA warning letter
ResearchAndMarkets.com

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FDA Roundup: January 7, 2025 - PR Newswire

Added to Collection on: 2025-01-07 21:15:41

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Food and Drug Administration
Center for Biologics Evaluation and Research
Medical device
Center for Drug Evaluation and Research
Dietary supplement
Federal Food, Drug, and Cosmetic Act
Good tissue practice
Form FDA 483

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New Year, Same Challenges: Pharma's Ongoing Struggle with FDA 483s - PharmTech

Added to Collection on: 2025-08-28 18:26:35

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Food and Drug Administration
Form FDA 483
Good manufacturing practice
FDA warning letter
Office of Global Regulatory Operations and Policy

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PDA 2025: How Strategic CAPA Builds Anti-Fragile Manufacturing Compliance

Added to Collection on: 2025-09-12 16:34:11

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Food and Drug Administration
Form FDA 483
Biopharmaceuticals
Corona Borealis
Biomanufacturing
Corona
Gooen Bizjak
Tara Gooen Bizjak

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Inside Warning Letters: A Statistical Update - Food and Drug Law Institute (FDLI)

Added to Collection on: 2025-10-03 19:12:02

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Food and Drug Administration
FDA Center for Devices and Radiological Health
Form FDA 483
WLS-TV
Center for Drug Evaluation and Research
Direct-to-consumer advertising
WLS-FM

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