Bouchra O completed this course and earned a Pharmuni certificate.

Certificate Registration No.: 12 100 60610 TMS
Dive into the foundations of Good Documentation Practices (GDocP) in the pharmaceutical and life sciences industries. The course explains why documentation is a cornerstone of data integrity, product quality, and regulatory compliance in GxP environments, and how GDocP supports reliable, traceable, and trustworthy records.
You will gain a clear understanding of how GDocP relates to GMP, ISO standards, and regulatory expectations, and why accurate, contemporaneous, and controlled documentation is essential for audits, inspections, and routine operations.
The course focuses on key elements of GDocP in practice, including:
• The ALCOA and ALCOA+ principles of data integrity
• How Document Control manages the lifecycle of controlled documents
• How to create, correct, and maintain compliant records in everyday work
Through practical explanations and workplace examples, this course helps learners understand what good documentation looks like in real GxP environments, why it matters, and how their own record-keeping affects quality and compliance. It is best suited to professionals who need a clear foundational understanding of documentation requirements in regulated work.
This course has been desgined with learning objectives at the heart of it, so you can be assured to walk away with a valuable new knowledge set. After completing this course, you will be able to: