A STUDY ON EFFECTIVENESS OF QUALITY ASSESSMENT MECHANISM OF VERITY PHARMACEUTICALS KULAPPULLY

This article explores the quality assessment mechanisms at a pharmaceutical company in India, emphasizing its role in ensuring product safety, efficacy, and compliance with regulatory standards. The Indian pharmaceutical industry, a global leader in generic drug production, faces significant regulatory scrutiny and quality expectations. This study delves into the company's comprehensive quality management system (QMS), highlighting processes such as raw material inspection, in-process quality control, and finished product testing. Utilizing a mixed-methods approach, including surveys, interviews, document analysis, and case studies, the research identifies strengths such as robust Standard Operating Procedures (SOPs), advanced technology utilization, and regular employee training. However, areas for improvement, including documentation efficiency, cross-departmental communication, and resource allocation, are also discussed. The article provides strategic recommendations for digital transformation, enhanced training, improved communication channels, investment in technology, and resource optimization. Ultimately, the study underscores the importance of continuous improvement in maintaining high quality standards and sustaining the company's competitive edge in the dynamic Indian pharmaceutical landscape.