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Updated in [July 27th, 2023]
This course provides learners with an understanding of the data integrity requirements for pharmaceuticals. It covers topics such as GMP principles, FDA and European inspector citations, US Warning Letters and EU Non-Compliance Reports, and international authority guidelines. The learning objectives are to enable learners to understand the data integrity requirements of a GMP regulated laboratory in pharmaceutical organisations and contract labs, and how laboratory personnel can ensure compliance and be able to defend their positions. The course also covers basics in data integrity and audit trail review, as well as the differences between good documentation Practices requirements and data integrity requirements. Specialised sessions focus on data integrity requirements for analytical laboratories and Microbiology laboratories. The course focuses only on hybrid and electronic systems and does not consider paper-based data integrity.
Course Syllabus
Data Integrity Requirements for Pharmaceuticals