Item no.
USP-CM-231-05-02
Unit
Each
Shipment details
No Dangerous Good
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Description
This course discusses revisions made to USP-NF General Chapters <232> Elemental Impurities-Limits and <233> Elemental Impurities-Procedures. In addition to discussing the changes and why they are necessary, this course will cover the implementation timeline, how limits apply to products, and a brief method description. This course also includes a discussion on the draft guidance published by the Food and Drug Administration (FDA) in June 2016 and the implementation timeline that has led to the current standards.<br>There will be a knowledge assessment at the end of the course. If this course is taken as part of the USP certificate program, you will be required to pass this knowledge assessment with a score of 80 percent to determine if your comprehension of the topics presented meets USPs minimum requirements
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