WHO-GMP

GMP: Good Manufacturing Practices for Quality Standards

Good Manufacturing Practices (GMP) is a system of processes, procedures, and documentation that help ensure that products are consistently produced and controlled according to quality standards. These practices are required in order to conform to guidelines and regulations recommended by agencies that control authorization and licensing for the manufacture and sale of food, drug products, and active pharmaceutical products.

GMP guidelines and regulations require that manufacturers, processors, and packagers of drugs, medical devices, and food take proactive steps to ensure that their products are safe, pure, and effective. GMP guidelines and regulations address many issues that can influence the safety and quality of a product. Some of these are:

Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls.
Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls.

GMP applies to organizations that manufacture and process drugs, cosmetics, medical products, and food. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls.

Organizations that meet GMP or cGMP (current Good Manufacturing Practices) will not only comply with the legislation, but also will commit to a program which will substantially increase the quality of their product and increase revenues and customer satisfaction. Some other benefits of implementing GMP are:

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