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.
Strategic thinking is a must-have skill for lab managers. At the 2025 Lab Manager Leadership Summit, Christie Bowden shared insight for developing that skill