About
This practical course explores how AI can be used to create, improve, and manage GMP documentation more efficiently while maintaining quality, consistency, and regulatory compliance. Participants will learn how to apply AI to common documentation tasks such as drafting SOPs, protocols, work instructions, reports, and other controlled documents. The course covers practical techniques for generating document structures, improving clarity and consistency, identifying missing information, standardizing terminology, and supporting document review and revision. Participants will also learn the importance of human oversight, document control, data integrity, and appropriate use of AI within GxP-regulated environments. Designed for professionals in pharmaceutical, biotechnology, quality assurance, quality control, manufacturing, and laboratory operations, this course provides practical methods for using AI to reduce repetitive documentation work, accelerate SOP development, and improve overall documentation quality without compromising GMP requirements.
You can also join this program via the mobile app. Go to the app