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Description

"A revision of the former “Dissolution: Theory and Best Practices"" course, this one-day course will emphasize the fundamentals of dissolution testing of solid oral dosage forms and address specifics related to the qualification of USP dissolution apparatus 1 and apparatus 2. Specifically, this course is dedicated to dissolution theory and the guidance presented in USP?NF General Chapter <711>, the handling of dissolution data and the qualification of an apparatus to prove its suitability for use.<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 USP’s minimum requirements."

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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