Item no.
USP-CM-231-05-01
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 presenting and discussing the necessary changes, a brief description of methods and how limits apply to products will be addressed in the course. The guidance published by the Food and Drug Administration (FDA) in June 2016 and the implementation timeline that has led to the current standards will be discussed along with risk-based approach.
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