GMP or Good Manufacturing Practice is a term that is recognized worldwide for the control and management of manufacturing and quality control testing of foods and pharmaceutical products.
GMP is that part of quality assurance which ensures that products are consistently manufactured and controlled to the quality standards appropriate to their intended use. It is thus concerned with both manufacturing and quality control procedure.
GMP regulations address issues including record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation and complaint handling. GMP is a good business tool which will help to refine both compliance and performance of a company.
GMP is the regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug and Cosmetic Act. These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective.
Importance of GMP:
GMP is the only key factor for successful manufacturing plant can lead the proper fulfillment of both inventors & consumers GMP ensures-
Purity of raw materials.
Consistency of supply & preservation.
Proper & skilled manpower for all the respective section.
Recent technology & product design.
Required quality, supply & marketing.
Product recall & proper counter actions.
Proper waste management.