Using Core-Shell Technology to Improve HPLC Methods within USP: Part 1

U.S. Pharmacopeia

Harnessing the Power of Core-Shell Technology to Improve Older, Validated HPLC Methods Within Acceptable USP Guidelines Part One: Quality Control Methods Guest Author: Dr. Jeff Layne Hello everyone, I hope Continue Reading

Allowable Adjustments to Pharmacopoeia Methods: Simplified Version

Effective August 2014, the United States Pharmacopoeia and the National Formulary published the latest revision to General Chapter on Chromatography that further clarifies what “allowable adjustments” can be made to USP methods without having to revalidate these methods.