Item no.
USP-CM-1088-01
Unit
Each
Shipment details
No Dangerous Good
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Description
This course provides an in-depth overview of IVIVC by exploring the relationship between the physicochemical and pharmacokinetic properties of a drug substance and a drug product. The correlation can help predict in vivo performance of a pharmaceutical dosage form based on its in vitro performance-an important basis for setting biorelevant specifications in line with the efficacy and safety of a drug product. This course will also include a short review of dissolution theory, in vitro data requirements, equipment qualification, and method validation, as described in USP-NF General Chapters <711>, <724>, and <1092>
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
View all available product details e.g. description, analytes/parameters, CAS Number, concentrations/values, sales unit/product format, method, source, transport information
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