Process and Cleaning Validation Define the terms – ‘validation’, ‘commissioning’, ‘qualification’ and ‘verification’ Give an overview of the specification, design, and verification approach for equipment systems associated with the pharmaceutical, biopharmaceutical and medical device industries.
End-of-Module Assignment Your end-of-module assignment is to clearly demonstrate your Knowledge and Understanding of the Quality Culture necessary to work in a GMP-regulated manufacturing environment, and that you personally understand the rules that govern manufacturing, the guidelines as to how the rules are applied, and the risk management tools to make scientific-based decisions. Assignment Requirements: […]