Mar 02 2021 Read 924 Times
ChroZen USP 467 Player is the optimised system for determination of residual solvents by fully complying with USP 467 and verifies the validity of analysis results for each analysis method.
For pharmacopeial purposes, residual solvents in pharmaceuticals are defined as organic volatile chemicals that are used or produced in the manufacture of drug substances or excipients, or in the preparation of drug products. Because these solvents can be harmful to human body if they remain in the final products, it is required to regulate these compounds not to exceed the specific limits defined in certain regulations.
United Stated Pharmacopeia (USP) classifies the residual solvents into Class Ⅰ, Class Ⅱ and Class Ⅲ depending on their risk to human health and USP 467 test method describes all the requirements for the analysis of residual solvents.
FPIs in defaulted corporate bonds will be exempt from the short-term limit and the minimum residual maturity requirement under the Medium Term Framework (MTF).At p
FPIs in defaulted corporate bonds will be exempt from the short-term limit and the minimum residual maturity requirement under the Medium Term Framework (MTF).At p