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Description
The USP Certificate of Pharmacopeial Quality Assessment?Dissolution Track offers the U.S. pharmaceutical Industry a comprehensive online program that highlights the knowledge and skills the quality assessment professional should have in order to comply with U.S. regulatory standards and the knowledge and skills required to be aligned with Good Manufacturing Practices. Designed and taught by the experts who help establish relevant USP-NF standards, the USP certificate program has three tracks each with eight courses. The courses in this program were carefully selected by USP scientists to provide a long lasting theoretical foundation and feature practical applications so you can have an immediate impact on your job and take your career to the next level. Certificate participants will have six months from the date of purchase to complete the program.
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