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Results for tag: "FDA Form 483"

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FDA Inspection (Recorded) - Product Thumbnail Image

FDA Inspection (Recorded)

  • Training
  • June 2024
  • 2 Days
  • Global
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FDA Inspection Preparedness and Compliance (December 2-3, 2025) - Product Thumbnail Image

FDA Inspection Preparedness and Compliance (December 2-3, 2025)

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  • December 2025
  • 2 Days
  • Global
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FDA Inspection Preparedness and Compliance (Recorded) - Product Thumbnail Image

FDA Inspection Preparedness and Compliance (Recorded)

  • Training
  • May 2025
  • 2 Days
  • Global
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FDA Inspection Preparedness and Compliance (September 3-4, 2025) - Product Thumbnail Image

FDA Inspection Preparedness and Compliance (September 3-4, 2025)

  • Training
  • September 2025
  • 2 Days
  • Global
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Good Documentation Practices - Webinar (Recorded) - Product Thumbnail Image

Good Documentation Practices - Webinar (Recorded)

  • Webinar
  • May 2022
  • 1 Hour
  • Global
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Establishing a Robust Data Integrity Program - Webinar (Recorded) - Product Thumbnail Image

Establishing a Robust Data Integrity Program - Webinar (Recorded)

  • Webinar
  • February 2019
  • 90 Minutes
  • Global
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The FDA Form 483 market is a subset of the pharmaceutical manufacturing industry. It is a regulatory document issued by the U.S. Food and Drug Administration (FDA) to a pharmaceutical manufacturing facility after an inspection. The form is used to document any observed violations of the FDA's Current Good Manufacturing Practice (CGMP) regulations. It is a critical tool for the FDA to ensure that pharmaceutical products are safe and effective. The FDA Form 483 market is composed of pharmaceutical manufacturers, contract manufacturers, and other related companies. Companies in this market include Pfizer, Merck, Novartis, GlaxoSmithKline, Sanofi, Johnson & Johnson, AstraZeneca, Bristol-Myers Squibb, and Eli Lilly. Show Less Read more

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