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Results for tag: "GMP"

Reviewing Drug Product Batch Records - Product Thumbnail Image

Reviewing Drug Product Batch Records

  • Training
  • 60 Minutes
  • Global
Good Laboratory Practice Regulations - Product Thumbnail Image

Good Laboratory Practice Regulations

  • Training
  • 75 Minutes
  • Global
CGMP controlled Raw Materials - Product Thumbnail Image

CGMP controlled Raw Materials

  • Training
  • 90 Minutes
  • Global
Good Documentation Guideline (Chapter <1029> USP) - Product Thumbnail Image

Good Documentation Guideline (Chapter <1029> USP)

  • Training
  • 60 Minutes
  • Global
Best Practices of Writing SOPs - Product Thumbnail Image

Best Practices of Writing SOPs

  • Training
  • 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