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Updated in [July 27th, 2023]
This course will provide an understanding of the different aspects of Good Laboratory Practices. Attendees will learn about data integrity in analytical and microbiology laboratories, including FDA/EU Citations, Non IT-Focus areas, IT-Focus areas, current trends of inspectors, and examples of data integrity. Additionally, the course will cover different guidelines on data integrity, evaluation of FDA warning letters and assessments, the ALCOA+ concept, audit trails in microbiology, and sterility tests. Furthermore, the course will cover analytical method validations, stability studies, out of specification and out of trend investigations, and common problem solving in analytical laboratories. The analytical method validation will include FDA expectations, QBD approach, QRM in analytical method validation, ICHQ14 - Analytical method development, ICHQ2(R1) - Analytical method validation, and overall evaluation and revalidation criteria. Finally, the course will cover human error investigation, including different types of human errors and how to investigate and avoid them.
Course Syllabus
Introduction