May 21, 2024 | By: Grady Wertman
This whitepaper focuses on the importance of disinfectant validations based on real-world conditions to maintain cGMP compliance in pharmaceutical manufacturing. It discusses the lack of specific testing requirements and the limitations of current testing methods and emphasizes the growing importance of site-specific surface testing.
Learn about the author below.
Study Director
Grady has worked at BioScience Laboratories for 8 years. He started in December 2013 as a laboratory technician without any lab experience, but since that time he has become a study director (Study Director III once integrated into Nelson Laboratories). He has made it his goal to learn and deeply understand any and all methods utilized. Grady holds undergraduate degrees in Cellular Biology/Neuroscience and Microbiology from the Montana State University – Bozeman. In his free time, he enjoys spending time with his family and cooking anything on his Traeger, while enjoying the requisite beverage(s), of course.
