Identification and Determination of Potential Impurities Present in the Acyclovir Drug Substance by GC-MS

By  

Current Pharmaceutical Analysis, Vol. 13, Iss. 5, 2017-08 ,pp. : 473-480

Bentham Science Publishers

Access to resources Recommend Favorite

Development and Validation of an HPLC Method for Quantitative Determination of Seven Impurities in Orlistat Capsules and Characterization of Two Novel Impurities

By  

Current Pharmaceutical Analysis, Vol. 12, Iss. 3, 2016-08 ,pp. : 198-207

Bentham Science Publishers

Access to resources Recommend Favorite

Validation of a RP-HPLC method for the assay of formoterol and its related substances in formoterol fumarate dihydrate drug substance

By Akapo S.O.   Asif M.  

Journal of Pharmaceutical and Biomedical Analysis, Vol. 33, Iss. 5, 2003-12 ,pp. : 935-945

Elsevier

Access to resources Recommend Favorite

Isolation and Identification of Impurities in the Parent Substance of Echinochrome and in the Drug Histochrome

By  

Pharmaceutical Chemistry Journal, Vol. 38, Iss. 1, 2004-01 ,pp. : 50-53

Springer Publishing Company

Access to resources Recommend Favorite

Method Validation and Measurement of Biomarkers in Nonclinical and Clinical Samples in Drug Development: A Conference Report

By Lee Jean W.   Weiner Russ S.   Sailstad Jeff M.   Bowsher Ronald R.   Knuth Dean W.   O’Brien Peter J.   Fourcroy Jean L.   Dixit Rakesh   Pandite Lini   Pietrusko Robert G.   Soares Holly D.   Quarmby Valerie   Vesterqvist Ole L.   Potter David M.   Witliff James L.   Fritche Herbert A.   O’Leary Timothy   Perlee Lorah   Kadam Sunil   Wagner John A.  

Pharmaceutical Research, Vol. 22, Iss. 4, 2005-04 ,pp. : 499-511

Springer Publishing Company

Access to resources Recommend Favorite