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Copyright @ B&W TEK Overview of the NanoRam Handheld Raman for Rapid Material Identification B&W Tek, Inc Newark, DE USA September 2013.
1 ASTM International Committee F40 on Declarable Substances in Materials Department of Commerce 2009 January 13.
PHARMACEUTICAL VALIDATION 1. VALIDATION 2 The U.S FDA defines Process Validation as, “It is an establishing documented evidence which provides a high.
1b_RHI Clasil Plant
ASTM International Committee F40 on Declarable Substances in Materials
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Advantages of Handheld Raman in the Pharmaceutical Industry: Meeting PIC/S Requirements Dr. Katherine A. Bakeev B&W Tek, Inc Newark, DE USA September 24,
