Item no.
USP-CM-231-03
Unit
Each
Shipment details
No Dangerous Good
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Description
This two-day theory and lab course will prepare you for the implementation of USP Elemental Impurities standards. This course will emphasize hands-on learning of sample preparation and elemental impurities analyses of pharmaceutical materials per USP-NF General Chapters <232> and <233>. The first day will be dedicated to classroom learning on elemental impurities analysis, including risk-based analysis, calculation of J concentrations and working calibration standards, and calculation of accuracy, sensitivity, repeatability, and ruggedness. The second day will be a laboratory practical using closed-vessel microwave digestion and ICP-MS or ICP-OES to prepare and analyze representative samples.
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
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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