About
This practical course introduces the essential principles of document management and Electronic Document Management Systems (EDMS) for life sciences organizations. Participants will learn how to create, review, approve, distribute, revise, archive, and control documents throughout their lifecycle in a structured and compliant environment. The course covers key topics including document lifecycle management, version control, approval workflows, electronic signatures, audit trails, access control, document traceability, and regulatory requirements. Practical examples demonstrate how EDMS can replace fragmented file-based processes and improve collaboration, compliance, and operational efficiency. Designed for professionals in pharmaceutical, biotechnology, medical device, research, quality assurance, and regulated environments, this course provides practical knowledge for implementing and operating effective digital document management processes.
You can also join this program via the mobile app. Go to the app