Under the Revised Schedule M, Good Documentation Practices (GDP) have become even more critical to ensure data integrity, regulatory compliance, and traceability across all pharmaceutical operations. This course is designed to help professionals involved in manufacturing, quality assurance, and regulatory functions master the updated documentation requirements as per CDSCO guidelines.

You’ll gain practical knowledge on how to create, review, manage, and archive documents in a way that meets both national and international GMP standards. Learn how to avoid common documentation errors, implement ALCOA+ principles, and maintain a robust, inspection-ready documentation system.