The Online Services portal gives customers of AAIPharma Services the flexibility to select the pharmacopeia, material and tests from a database; enter the number of preparations, special instructions ...
USP plans to release a new version of the Chapter 1226. This seminar will provide all information on existing and new USP and FDA requirements. Attendees will also receive strategies and tool kits ...
The new <1226>, 'Verification of Compendial methods' was published in second supplement to USP 30 - NF 25 (2007) and is now official. Compliance to USP <1226> is one of the FDA requirements for ...
Natural cyclodextrins (CDs) and their synthetically modified forms, hydroxypropyl-β-cyclodextrin (HP-β-CD) and sulfobutyl-β-cyclodextrin (SB-β-CD), are critical components in pharmaceutical ...
The process of method modernization, which involves integrating advancements in system and column technology for routine analysis, is a challenge many regulated laboratories face due to a larger focus ...
The authors discuss a new approach to address globally harmonized compendial standards. Twenty-first century challenges require 21 st century solutions. This fact applies broadly in our current global ...
In-house harmonization of excipient specifications ensures compliance with multiple pharmacopoeias, reducing redundant testing and aligning with global regulatory expectations. Specification ...
DUBLIN--(BUSINESS WIRE)--The "Analytical Method Validation, Verification and Transfer Virtual Seminar (Oct 7th - Oct 9th, 2025)" has been added to ResearchAndMarkets.com's offering. Dependable ...
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