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Results for tag: "GMP"

How to Withstand an FDA Audit of your Facility - Product Thumbnail Image

How to Withstand an FDA Audit of your Facility

  • Training
  • 60 Minutes
  • Global
Life Cycle Validation of GMP Potency Bioassays - Product Thumbnail Image

Life Cycle Validation of GMP Potency Bioassays

  • Training
  • 90 Minutes
  • Global
Good Documentation Practices for GXPs - Product Thumbnail Image

Good Documentation Practices for GXPs

  • Training
  • 60 Minutes
  • Global
Overview of Quality by Design - Product Thumbnail Image

Overview of Quality by Design

  • Training
  • Global
Creating FDA-compliant cGMP Training Program - Product Thumbnail Image

Creating FDA-compliant cGMP Training Program

  • Training
  • 60 Minutes
  • Global
HPLC Method Development and Validation - Product Thumbnail Image

HPLC Method Development and Validation

  • Training
  • 60 Minutes
  • Global
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Reviewing Drug Product Batch Records - Product Thumbnail Image

Reviewing Drug Product Batch Records

  • Training
  • 60 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