{"title":"Dissolution Testing in Generic Drug Development:\n \n Methods,\n \n \n Requirements,\n \n \n and\n \n \n Regulatory\n \n \n Expectations/Requirements","authors":"","doi":"10.1002/9781119634645.ch13","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":376406,"journal":{"name":"Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence","volume":"8 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/9781119634645.ch13","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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