Abstract

Good Manufacturing Practices (GMP) are essential regulatory guidelines that ensure the production of pharmaceutical products with consistent quality, safety, and efficacy. GMP establishes a framework for pharmaceutical manufacturers to follow stringent operational standards, offering systematic processes designed to minimize risks such as contamination, cross-contamination, and variability in the production process. As an integral component of pharmaceutical quality control (QC), GMP plays a critical role in maintaining product integrity and patient safety. This article examines the importance of GMP in pharmaceutical quality control, highlighting its principles, implementation, benefits, challenges, and the evolving role of GMP in the global pharmaceutical industry. By understanding the significance of GMP in QC, it is possible to appreciate how these practices contribute to improved drug development, manufacturing efficiency, and regulatory compliance in the industry.