Disinfectant
qualification studies play a key role in assuring that a company's clean room
is sterile and within the prescribed U.S. Food and Drug Administration (FDA)
standards. With clean room sterility of utmost importance, disinfectant
qualification studies are valuable in analyzing and evaluating disinfectant
effectiveness.
To
examine this important subject further, Microtest have produced a white paper
written by Deborah Ensign, Shawn Sherry, and Kate Bloomrose. The paper covers
some of the basic areas.
Posted by Tim Sandle
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