A Review on Evolution of Good Manufacturing Practices in the Pharmaceutical Industry

Good manufacturing practices (GMP) is a part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization. GMP guidelines provide minimum requirements for pharmaceutical or a food product manufacturer must meet to assure that the products are of high quality and do not pose any risk to the consumer or public. Good Manufacturing Practices is part of quality assurance that ensures that products are regularly produced and checked to meet quality standards and marketing authorizations for their intended use. These standards set minimum standards for pharmaceutical or food manufacturers to provide quality, safe products for consumers and society. A component of quality assurance known as “good manufacturing practices” guarantees that goods are continuously produced and controlled to the quality requirements relevant to their intended use and as mandated by the marketing license. GMP rules provide minimum standards that manufacturers of food or pharmaceutical items must fulfill to ensure that their products are safe for consumers and do not pose any risks. The safety and effectiveness of medical products are dependent on the healthcare industry upholding high standards of quality. The manufacture, control and quality assurance of medicines, medical devices and other healthcare items are made easier with the support of a system of rules and regulations known as good manufacturing practices or GMPs. In order to protect patient health and uphold public confidence this research study examines the importance of GMP in the healthcare sector.