Streamlining the Analysis of Oral Contraceptives Using the ACQUIT Y UPLC H-Class System

[ APPLICATION NOTEBOOK ] IMPURITIES Developing Safe and Effective Drugs INT RODUCTION NAVIGATION T he pharmaceutical industry is integral in maintaining public health by providing therapeutic and preventative medicines. T he cornerstones of bringing new medicines to market are quality,…

USP Method Transfer of Levonorgestrel and Ethinyl Estradiol Tablets from HPLC to UPLC Mia Summers and Kenneth J. Fountain, Waters Corporation, 34 Maple St., Milford, MA, USA A P P LIC AT ION BEN EFIT S n Updating USP methods…

[ APPLICATION NOTEBOOK ] METHOD DEV ELOPMENT The Path to Successful Drug Development Starts with Purposeful Method Development [ INTRODUCTION ] T he Path to Successful Drug Development Starts with Purposeful Method Development The goal of method development in pharmaceutical…

FUTURE-PROOF SOLUTIONS FOR REGULATED LABORATORIES IN THE FACE OF CHANGING USP <621> GUIDELINES How to use UPLC technology within “allowable adjustments” to improve QC laboratory throughput For many in the regulatory environment, the collection of standards provided by the United…