In the pharmaceutical and biotechnology industries, Corrective and Preventive Actions (CAPA) are fundamental to maintaining compliance with regulatory standards and ensuring product quality. For professionals in pharma QA or those pursuing quality assurance training, understanding CAPA processes is vital to resolving issues, preventing recurrence, and driving continuous improvement. AAPS’s upcoming webinar, Developing an Effective CAPA Strategy, will dive deep into effective CAPA practices, equipping participants with actionable insights to enhance organizational quality and compliance. Understanding CAPA and Its Importance CAPA is the backbone of a robust Quality Management System (QMS). It provides a structured approach to identifying root causes, addressing.. READ MORE »
The journey from dream to reality for students eager to enter the Canadian pharmaceutical industry can often feel daunting. The road is challenging between adjusting to a new country and building a career in a competitive Pharma QA market. But with the right guidance, it’s also incredibly rewarding. At the Academy of Applied Pharmaceutical Sciences (AAPS), we don’t just prepare students for the industry; we empower them to succeed. Meet Parnian Dokouhaki, a Pharmaceutical QAQC Program graduate who now works in the Quality Assurance (QA) department at Eurofins. Her journey from student to professional is a powerful example of what’s.. READ MORE »
Are you a pharmaceutical quality assurance professional seeking to strengthen your expertise in out-of-specification (OOS) investigations within testing labs? This critical area of QA can be challenging yet essential for ensuring product quality and regulatory compliance. Join us on November 14, 2024, for a comprehensive workshop on mastering OOS investigations explicitly designed for professionals like you. Why This Workshop Is Essential OOS results are a top priority for regulatory authorities. When test results fall outside predefined specifications, it’s not simply a “red flag” but a call for immediate and thorough investigation to maintain product integrity and regulatory compliance. Effective OOS.. READ MORE »
