16:00 - 18:00 (CET) at 15 February 2025
Quality Management Systems (QMS) in GMP: Key Principles for Compliance and Continuous Improvement
with Humzaa Imtiaz Ullah
$60

Webinar Description
What you will learn?
A well-structured Quality Management System (QMS) is the backbone of GMP compliance, ensuring that products are consistently manufactured to meet quality and regulatory standards. This webinar explores the fundamental components of QMS, including Change Control, Deviation Management, CAPA, and Documentation Control. Attendees will gain insight into how a strong QMS helps identify, correct, and prevent quality issues, while also improving operational efficiency and regulatory compliance.
By the end of this webinar, participants will be able to:
Understand the Role of QMS in GMP Compliance – Learn how a robust QMS helps maintain product quality, ensures regulatory adherence, and supports continuous improvement in manufacturing and quality control processes.
Explore Key Components of QMS – Gain an overview of core QMS elements such as Change Control, Deviation Management, CAPA, and internal audits, and understand how each component contributes to overall product quality and safety.
Recognize the Importance of Change Control – Understand how controlled changes in processes, equipment, and documentation help maintain consistency and prevent unintended quality risks.
Learn How to Handle Deviations and Non-Conformances – Identify what constitutes a deviation, how to document it properly, and the importance of root cause analysis in preventing recurrence.
Implement Effective CAPA Procedures – Understand the principles of Corrective and Preventive Actions (CAPA), how to investigate quality issues, and the steps required to implement lasting improvements.
Ensure Proper Documentation and Record-Keeping – Discover the significance of Good Documentation Practices (GDP) and how accurate, well-maintained records support compliance, traceability, and audit readiness.
Guest Speaker

The speaker for today’s webinar is Humzaa Imtiaz, who holds a Master’s degree in Chemical Engineering. With a strong academic foundation, he has built a career in the pharmaceutical industry, gaining valuable hands-on experience in Good Manufacturing Practices (GMP) and Quality Management Systems (QMS). He has worked in key roles such as Supplier Quality Engineer, Quality System Engineer, and Project Lead, where he has been instrumental in ensuring compliance, optimizing quality systems, and driving process improvements. His expertise spans various aspects of GMP implementation, regulatory compliance, and quality assurance in industrial settings. Therefore, we are grateful to have him with us for this webinar to share his insights and experiences.