11 December 2025 || 18:00 - 19:30 (CET)
Good Documentation Practice within GMP
Humzaa Imtiaz Ullah
$20
Webinar Description
What you will learn?
Proper documentation is the backbone of Good Manufacturing Practices (GMP), playing a vital role in ensuring product integrity, regulatory compliance, and operational efficiency. This webinar provides a comprehensive overview of best practices in GMP documentation and record-keeping, including Good Documentation Practices (GDP), batch manufacturing records, Standard Operating Procedures (SOPs), and audit readiness. Attendees will gain insights into the importance of accurate, consistent, and well-maintained records, common documentation errors to avoid, and strategies for ensuring compliance with global regulatory requirements. This session is ideal for professionals involved in manufacturing, quality assurance, and regulatory affairs who want to enhance their documentation practices and maintain an effective Quality Management System (QMS).
By the end of this webinar, participants will be able to:
Understand the Role of Documentation in GMP Compliance – Learn why proper record-keeping is essential for ensuring product quality, regulatory adherence, and maintaining a traceable history of manufacturing activities.
Apply Good Documentation Practices (GDP) – Gain an understanding of GDP principles, including accuracy, legibility, completeness, and timely recording, to ensure compliance with GMP requirements.
Maintain Accurate and Complete Batch Records – Learn how to properly document batch manufacturing records, including critical data points that support traceability, deviation handling, and product release.
Develop and Manage Effective Standard Operating Procedures (SOPs) – Understand the importance of clear, well-written SOPs and how they serve as essential tools for training, process standardization, and regulatory inspections.
Ensure Audit-Ready Documentation – Discover best practices for organizing, reviewing, and maintaining records to ensure they meet regulatory expectations and are readily available for internal and external audits.
Identify and Prevent Common Documentation Errors – Recognize frequent mistakes in GMP documentation, such as missing signatures, incomplete records, and improper corrections, and learn how to prevent them through proper training and oversight.
Guest Speaker
Humza Imtiaz is a Chemical Engineer with diverse experience across quality assurance, procurement, and business development in the pharmaceutical and cement industries. Currently working as a Document Manager within Engineering Management. As the founder of Chemical Engineering Life, he has led global initiatives in mentorship and professional development for engineers. With a strong background in data analysis, stakeholder management, and project leadership, Humza brings both technical expertise and a passion for helping others grow in their careers.