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Description

This hands-on bioassay laboratory-based course focuses on USP General Chapters <1030>, <1032>, <1033> and <1034> along with laboratory execution of bioassay procedures. In this highly interactive course, participants will learn key concepts of in vitro bioassays, including use of relevant terminology, best practices, design, development, validation, post-validation, analysis, interpretation and reporting of results. It’s a great opportunity for those who wish to understand the best practices for analysis and consistent interpretation of data obtained from method development and validation. Scientists also gain hands-on laboratory experience and learn about the application of appropriate statistical tools for data analysis. (Event Laboratory 40 hours)

Miscellaneous

Certificate of Analysis (specimen)

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Product data sheet

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USP | United States Pharmacopeia

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