Good manufacturing practice (GMP) is a system for ensuring that manufacturers produce goods consistently and in a controlled way. Companies and organizations must produce their goods according to quality standards. GMP contains basic preventive guidelines for factory and facility operations. In other words, it is part of a system that aims to maintain high standards. It aims to minimize risks that we cannot eliminate through testing the final products.
Good manufacturing practices are the guidelines that regulatory agencies recommend for the producers and sellers of drugs and active pharmaceutical products. The guidelines are also recommendations for the manufacturers and sellers.
A good manufacturing practice (GMP) is one that conforms to the guidelines set by the regulatory agencies that control authorization and licensing for the production and sale of active pharmaceutical products.
These guidelines provide minimum requirements that a manufacturer must meet to assure that their l are well trained, and that the product has been checked for quality more than just at the end phase. GMP is typically ensured through the effective use of a quality management system (QMS).