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Results for tag: "GMP"

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FDA Inspection (Recorded) - Product Thumbnail Image

FDA Inspection (Recorded)

  • Training
  • June 2024
  • 2 Days
  • Global
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The Latest Updates in Global GMP (July 8, 2026) - Product Thumbnail Image

The Latest Updates in Global GMP (July 8, 2026)

  • Training
  • July 2026
  • 90 Minutes
  • Global
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FDA's 21 CFR Part 11 Add-on Inspections (Recorded) - Product Thumbnail Image

FDA's 21 CFR Part 11 Add-on Inspections (Recorded)

  • Training
  • January 2026
  • 90 Minutes
  • Global
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Good Manufacturing Practice (GMP) is a set of regulations and guidelines that govern the production of pharmaceuticals. GMP is designed to ensure that pharmaceuticals are consistently produced and controlled according to quality standards. It is intended to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Compliance with GMP is mandatory for all manufacturers of pharmaceuticals and active pharmaceutical ingredients. The GMP market is composed of companies that provide services and products related to GMP compliance. These services and products include consulting, auditing, training, and software solutions. Companies in the GMP market include Parexel, SGS, Eurofins, and NSF International. Show Less Read more