Item no.
USP-CM-711-03
Unit
Each
Shipment details
No Dangerous Good
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Description
This two-day theory and laboratory course will emphasize the fundamentals of dissolution testing of solid oral dosage forms with a focus on the qualification of USP dissolution apparatus 1 and apparatus 2. The first day will be dedicated to classroom learning on 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. The second day will be a laboratory hands-on practice of the instrument qualification and conducting the Performance Verification Test (PVT).
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