Explore the types of stability chambers, required storage conditions, regulatory guidelines, and validation steps essential for pharmaceutical drug storage and testing.
Rethinking ventilation through filtration can help labs reduce emissions, cut energy costs, and meet institutional sustainability goals—without compromising safety
Learn how to prepare for and execute pharmaceutical QC lab audits. Discover types of audits, best practices, and strategies for responding to audit findings.
Explore how chanterelle mushrooms contribute to kokumi taste through fatty acid derivatives, using UHPLC-MS for compound identification and food quality control.
Discover how scientists extended fresh pasta’s shelf life by 30 days using innovative packaging and processing methods. Learn what it means for food safety.
Understand how to manage Out-of-Specification (OOS) results in pharmaceutical manufacturing. Learn about OOS definitions, investigation protocols, regulatory expectations, and corrective action strategies.
Discover the best practices for batch record review in pharmaceutical manufacturing. Learn about key components, review strategies, common errors, and compliance tips to ensure product quality and regulatory adherence.
Explore the fundamentals of Pharmaceutical Quality Assurance (QA), including its definition, scope, objectives, differences from Quality Control (QC), and key roles and responsibilities in regulated environments.