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Updated in [July 27th, 2023]
This course introduces learners to the regulatory requirements for computerized systems in the pharmaceutical industry and explores methods of meeting those requirements. It covers topics such as categorisation of software and hardware as per GAMP 5, different validation strategies, developing URS, FRS, FAT, SAT, IQ, OQ and PQ, test strategies, validation master plan and validation master report concept, and common questions and answers. This course is beneficial for regulatory, clinical, and IT professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors, as well as software vendors, auditors, and quality staff involved in GxP applications.
Course Syllabus
Computerised System Validation
Computerised System Validation