Pharmaceutical Quality Assurance and GMP

Ensuring drug safety, consistency, and compliance is the focus of this critical track. It begins with an overview of Good Manufacturing Practices (GMP) and the evolving landscape of international quality standards. Quality by Design (QbD) and Process Analytical Technology (PAT) will be discussed as modern tools for ensuring consistent product quality. Experts will share strategies for risk management, deviation control, and continuous improvement. Attendees will gain practical knowledge on quality audits, batch record review, and validation protocols. Emphasis will also be placed on data integrity and digital quality systems.

The session will cover post-approval changes, FDA warning letters, and CAPA (Corrective and Preventive Actions) best practices. Real-world GMP failures and success stories will offer actionable takeaways. This track is essential for professionals in manufacturing, QA/QC, and compliance, aiming to maintain excellence in pharmaceutical production and patient safety.

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