{"title":"仿制药开发中的溶出度检测:方法、要求和法规期望/要求","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":"{\"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}","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}
引用次数: 0