Pharmetric Laboratory recommends performing a USP 71 Method Suitability Test with the six organisms listed therein. This one time test is required if we cannot reference data via the Pharmetric Cross Reference Library. Once passing data has been confirmed, either through a full test or a Cross Reference, it is not necessary to perform the test again unless the formula changes or your batch size increase from the original.
IN EITHER CASE A FORMULATION SHEET IS REQUIRED FOR PHARMETRIC LAB TO TAKE ACTION.
Method Suitability Cross Reference Library; Ordering Instructions
Pharmetric Laboratory uses ATP Bioluminescence for rapid detection of microbiological contaminants in compounded sterile preparations
Meet the requirements of USP while harnessing the cutting-edge technology that allows for cost savings and speeds up the release of sterile preparations without sacrificing safety or reliability.
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