AGAWAM, Mass., June 2, 2014 (GLOBE NEWSWIRE) -- Manufacturers of sterile drug products are required by the FDA to undertake disinfectant qualification studies to determine the effectiveness of their disinfecting agents. A new white paper, “Disinfectant Qualifications: Insight and Perspective,” answers the most frequently asked questions about conducting a successful study. Download the paper from Microtest Laboratories at http://www.microtestlabs.com/disinfectant-qualifications.
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