Tag: facility and equipment guidelines

Understanding ICH Guidelines Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients (APIs)

Discover the significance of ICH Q7 guidelines in the pharmaceutical industry. Explore key aspects such as quality management, risk-based approaches, documentation requirements, and personnel training. Learn how adherence to ICH Q7 ensures global consistency and high standards in Active Pharmaceutical Ingredient (API) manufacturing. Stay informed about facility and equipment guidelines, change control practices, and more for robust pharmaceutical quality assurance.