Quality Risk Management in Pharmaceutical Industry

Author(s)	Ms. Pooja Ramdas Hatwar, Manali C. Asare, Jiterdra A. Kubde, Ravindra L. Bakal
Country	India
Abstract	The pharmaceutical sector functions under a highly regulated environment where patient safety and product quality are of utmost importance. Maintaining product consistency, ensuring regulatory compliance, and promoting continuous improvement all depend on a strong quality management system (QRM). The basic principles, elements, and legal framework that control QMS in the pharmaceutical industry are examined in this paper. Good Manufacturing Practices (GMP), risk management, GLP, TQM, QC and QA, maintenance, GLP and GMP, and auditing procedures are among the essential components that are highlighted.
Keywords	Quality management, Audits, maintenance.
Field	Medical / Pharmacy
Published In	Volume 7, Issue 4, July-August 2025
Published On	2025-07-27
DOI	https://doi.org/10.36948/ijfmr.2025.v07i04.51788
Short DOI	https://doi.org/g9vpkd

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International Journal For Multidisciplinary Research