Abstract

Dr. Kaushal Kumar Samriya*, Dr. Devendra Singh Chahar, Dr. Rameshwar Lal and Dr. Sankalp Sharma

ABSTRACT

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. The fundamental tenets of GMP are examined along with the regulatory environment and its effects on medication production, quality assurance, product safety and regulatory compliance among other facets of the healthcare industry. In addition, the paper addresses the difficulties and prospects for GMP implementation in the future highlighting the necessity of continual improvements to satisfy the changing needs of the sector.