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Journal of Pharmaceutical and Biomedical Analysis|February 10, 2009
Identification of a process impurity formed during synthesis of a nevirapine analogue HIV NNRT inhibitor using LC/MS and forced degradation studiesFenghe Qiu, Scott Pennino, Carl A Busacca, et al.Journal of Pharmaceutical and Biomedical Analysis|January 24, 2013
Application of iChemExplorer in pharmaceutical pH stress testingFenghe Qiu, Lily Du, Ashish Soman, et al.Journal of Pharmaceutical and Biomedical Analysis|August 9, 2015
Monitoring the chemical and physical stability for tromethamine excipient in a lipid based formulation by HPLC coupled with ELSDShirley A Rodríguez, Fenghe Qiu, Michael Mulcey, et al.Pharmaceutical Development and Technology|November 9, 2021
Stability screening of pharmaceutical cocrystalsKenneth C Waterman, Alisa K Waterman, Teslin M Botoy, et al.Magnetic Resonance in Chemistry : MRC|September 6, 2005
Structure elucidation and total synthesis of a unique group of trace impurities in Tipranavir drug productCarl A Busacca, Scot Campbell, Anjan Saha, et al.The AAPS Journal|September 16, 2021
Considerations for Updates to ICH Q1 and Q5C Stability Guidelines: Embracing Current Technology and Risk Assessment StrategiesMegan E McMahon, Alexander Abbott, Yelizaveta Babayan, et al.The Journal of Organic Chemistry|August 4, 2004
Electronic control of chiral quaternary center creation in the intramolecular asymmetric heck reactionCarl A Busacca, Danja Grossbach, Scot J Campbell, et al.Pageof 1