Preparing for a GMP inspection requires organised records, trained staff, and consistent compliance across all departments. Companies must keep key documents—SOPs, batch records, training logs, and calibration reports—complete and accessible.... Read More
Author: Paul R Palmer
Standard Operating Procedures (SOPs) are essential for consistency, compliance, and quality in pharmaceutical operations. They provide clear, step-by-step instructions for critical processes, supporting staff training and regulatory adherence. Effective SOP... Read More
Integrating deviation data with Quality Risk Management (QRM) enables pharmaceutical companies to shift from reactive to proactive quality assurance. By analyzing trends, severity, and root causes, teams can identify high-risk... Read More
Leveraging kinetic and thermodynamic principles, pharma companies can enhance supply chain sustainability. Advanced technologies serve as the primary driver, while resilient systems and cross-functional collaboration ensure compliance with standards and... Read More