Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Judy P. Boehlert"'
Autor:
Judy P. Boehlert
Publisher Summary Identification, qualification, and quantification of impurities are critical tools for assessing the safety and quality of pharmaceutical drug substances and their associated dosage forms. Safety and quality, with respect to impurit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794f938ff9294ae987f3dfcf81c95196
https://doi.org/10.1016/s1464-3456(00)80007-1
https://doi.org/10.1016/s1464-3456(00)80007-1
Autor:
Judy P. Boehlert
Publikováno v:
Drug Development and Industrial Pharmacy. 10:1343-1371
Stability-indicating analytical methods are developed to monitor the stability of pharmaceutical dosage forms during the investigational phase of drug development, and, once the drug is marketed, for the ongoing stability studies which must be conduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bf817fde90389943caceb15a70797b4
https://doi.org/10.3109/03639048409039057
https://doi.org/10.3109/03639048409039057
Autor:
Gary L. Burce, Judy P. Boehlert
Publikováno v:
Journal of Pharmaceutical Sciences. 67:424-426
A stability-indicating assay for the degradation products of procarbazine hydrochloride was developed using high-pressure liquid chromatography. The method uses a buffered methanol-water mobile phase on a reversed-phase column. Concentrations of degr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0859e3e19813940ec26fa7a475827115
https://doi.org/10.1002/jps.2600670345
https://doi.org/10.1002/jps.2600670345