Item no.
USP-EXC-WS-03
Unit
Each
Shipment details
No Dangerous Good
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Description
To investigate changes in excipient grade and the impact of these changes on bioequivalence and bioavailability, FDA has an ongoing research program for generic drugs for various product categories to steer development of guidances and recommendations to industry on excipient selection for generic products. (Webcast 22 minutes)
Miscellaneous
Certificate of Analysis (specimen)
Reference Material CoA specimen: for the current lot, please contact your customer service representative at info@labmix24.com
Product data sheet
View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information
US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.
Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.
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- USP Reference Standards
- USP Pharmaceutical Analytical Impurities
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