GMP Deviation Breakthrough: Causes, Types, and Solutions
This article explores the critical causes, types, and actionable solutions for managing GMP Deviation in pharmaceutical manufacturing. Learn how to address deviations caused by human error or equipment failure and implement preventive measures to ensure product quality and regulatory compliance.
CAPA Drives Powerful Continuous Improvement Results
CAPA (Corrective and Preventive Action) is a vital tool for driving continuous improvement. By addressing root causes and implementing preventive measures, CAPA ensures lasting improvements, enhanced compliance, and operational efficiency across industries. Discover how CAPA fosters a culture of growth and accountability.