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cGMP Pharmaceutical Facilities

Good Manufacturing Practices (GMPs) are practices that have become regulations that describe the methods, equipment, facilities, and controls required for producing:

• Human pharmaceutical products and veterinary products
• Biologically derived products
• Medical devices, and
• Processed food

The "c" in cGMP stands for "current" Good Manufacturing Practices or regulations to emphasize the dynamic nature of the expectations associated.

In the United States, drug cGMPs were formally introduced in 1963 and significantly rewritten in the 1970’s. They are now controlled by the FDA (US Food and Drug Adminstration). Canadian drug GMPs exist in various forms in the 1950’s-1970’s before being published in their current form in the 1980’s.
(Source: cGMP.com, LearningPlus, Inc. & LearnWright, Inc.)

Related Articles:
cGMP.com - Great resource for information about cGMPs
FDA (Food & Drug Administration)
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