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cGMP

cGMP

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What is cGMP?

Current Good Manufacturing Practice (cGMP) is a system for ensuring that pharmaceutical products are consistently produced and controlled according to quality standards. It covers all aspects of production; from starting materials, premises and equipment to the training and personal hygiene of staff. The goal is to minimize risks such as contamination, mix-ups and errors. cGMP regulations are enforced by regulatory agencies like the FDA in the United States and similar bodies in other countries. Compliance with cGMP is mandatory for pharmaceutical manufacturers and ensures the safety, efficacy, and quality of drug products.

What other technologies are related to cGMP?

cGMP Complementary Technologies

cGLP (current Good Laboratory Practice) is related to quality control but focuses on laboratory practices, making it complementary to cGMP which focuses on manufacturing practices.
mentioned alongside cGMP in 90% (65) of relevant job posts
FDA guidelines provide the regulatory framework within which cGMP operates. Compliance with these guidelines is essential for cGMP.
mentioned alongside cGMP in 54% (64) of relevant job posts
The FDA is the regulatory body that enforces cGMP regulations. Therefore, it is directly related and complementary.
mentioned alongside cGMP in 8% (334) of relevant job posts

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