Abstract

Quality control is a critical aspect of drug development and manufacturing, ensuring the safety, efficacy, and reliability of pharmaceutical products. This article provides an overview of key strategies employed in quality control throughout the drug development and manufacturing processes. From comprehensive analytical testing to regulatory compliance and continuous improvement, these strategies contribute to the creation of high-quality pharmaceuticals. The article emphasizes the importance of adherence to Good Manufacturing Practices (GMP), risk-based approaches, data integrity, stability testing, and personnel competence. By adopting these strategies, pharmaceutical companies can enhance product quality, meet regulatory standards, and prioritize patient well-being