Good Documentation Practice (GDP) is at the heart of compliance and product quality in the pharmaceutical, biotech, and medical device industries. Accurate, complete, and legible records not only demonstrate that work was done correctly but also ensure traceability, accountability, and regulatory compliance.

From writing entries clearly and contemporaneously, to correcting errors properly, signing records responsibly, and safeguarding data integrity — GDP principles guide how we record and manage every critical step in the manufacturing and quality process.

This course provides learners with:

• A clear understanding of GDP principles and their role in regulatory compliance.

• Practical techniques for creating accurate, complete, and legible records.

• Interactive examples showing correct and incorrect documentation practices.

• Tips for avoiding common mistakes and ensuring data integrity at all times.

By following GDP best practices, learners will help their organization maintain regulatory compliance, protect product quality, and uphold patient safety.