Item no.
USP-CM-467-02
Unit
Each
Shipment details
No Dangerous Good
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Description
Significant revisions to standards for residual solvents found in USP?NF General Chapter <467> became official on July 1, 2008. These changes continue to impact the industry. In this one day course, both compendial and regulatory aspects will be covered. Additionally, different options and control strategies for implementation of analytical procedures A, B and C will be discussed. Other related topics including Validation <1225>, Verification <1226> and system suitability requirement and adjustment based on <621> will be highlighted. Furthermore, the most recent PF revision proposal and comparison of USP and EP procedures for residual solvent determination will briefly be reviewed.
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