Year: 2024
Type: article
Abstract: Quality assurance (QA) in the pharmaceutical industry is a critical function that ensures the safety, efficacy, and quality of pharmaceutical products. This article explores the multifaceted role of QA, encompassing compliance oversight, quality systems management, risk management, quality control testing, supplier and vendor management, and training and education. The QA department is instrumental in maintaining regulatory compliance, identifying and mitigating risks, and ensuring that products meet rigorous quality standards throughout their lifecycle. The future of QA is shaped by advancements in automation, artificial intelligence, advanced analytical techniques, continuous manufacturing, personalized medicine, and regulatory harmonization. These trends offer opportunities to enhance efficiency, accuracy, and reliability in quality assurance processes. Despite the challenges posed by regulatory changes, technological advancements, and globalization, QA remains a cornerstone of the pharmaceutical industry, dedicated to safeguarding public health and ensuring the highest standards of product quality. This comprehensive overview underscores the essential responsibilities and evolving landscape of quality assurance in the pharmaceutical sector.
Authors: Mayur Dandekar, Prajakta Dandekar
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W4410906319