Item no.
USP-CM-621-03-01
Unit
Each
Shipment details
No Dangerous Good
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Description
This course covers fundamentals of compendial HPLC including updates on related general chapter <621> Chromatography. In addition, Validation <1225>, Verification <1226> and Method Transfer <1224> will briefly be discussed. Furthermore, general chapter <1058> Analytical Instrument Qualification and its relation to above general chapters will be highlighted. ICH and FDA guideline and comparison to related USP general chapters will also be presented.
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