Item no.
USP-CM-231-01-1
Unit
Each
Shipment details
No Dangerous Good
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Description
"USP Education is pleased to offer its enhanced course, ""Impurities in Drug Substances and Drug Products-A USP Approach"". This course integrates ICH Guidance for impurities, relevant USP General Chapters, and current industry practices. It also provides insights and practical examples on how to evaluate and manage impurities in drug substances and drug products, and addresses the evaluation of contaminants, adulterants, foreign substances and impurities in drug substances and drug products, and packaging-related extractables and leachables. This course will cover USP-NF General Chapters <232>, <233>, <466>, <467> and <1086> and include case studies for impurities in the development and revision of USP monographs."
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.
As a USP-Authorized Distributor, we offer the following products and services:
- USP Reference Standards
- USP Pharmaceutical Analytical Impurities
- USP Training and educational programs