Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.Utilizing strategic thinking, risk-based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
This webinar describe, As part of the Case for Quality program US FDA noted how an excessive focus by the industry on co...
In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect of ma...
This course will educate you about various key elements of sterility assurance and contamination control such as Cleanro...
In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect of ma...
This course will educate you about various key elements of sterility assurance and contamination control such as Cleanro...
No advanced level courses available from Kelly Thomas at the moment.
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