{"title":"关于药物开发的简述","authors":"L. Roche","doi":"10.35248/0975-0851.21.S2.E002","DOIUrl":null,"url":null,"abstract":"Bioavailability is alluded to as the degree and rate to which the dynamic medication fixing or dynamic moiety from the medication item is ingested and opens up at the site of medication activity. The general bioavailability as far as the rate and degree of medication ingestion is viewed as prescient of clinical results. In 1984, the United States Food and Drug Administration (FDA) was approved to endorse conventional medication items under the Drug Price Competition and Patent Term Restoration Act dependent on proof of normal bioequivalence in drug assimilation through the direct of bioavailability and bioequivalence considers.","PeriodicalId":15184,"journal":{"name":"Journal of Bioequivalence & Bioavailability","volume":"32 1","pages":"1-1"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Short Note on Drug Development\",\"authors\":\"L. Roche\",\"doi\":\"10.35248/0975-0851.21.S2.E002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Bioavailability is alluded to as the degree and rate to which the dynamic medication fixing or dynamic moiety from the medication item is ingested and opens up at the site of medication activity. The general bioavailability as far as the rate and degree of medication ingestion is viewed as prescient of clinical results. In 1984, the United States Food and Drug Administration (FDA) was approved to endorse conventional medication items under the Drug Price Competition and Patent Term Restoration Act dependent on proof of normal bioequivalence in drug assimilation through the direct of bioavailability and bioequivalence considers.\",\"PeriodicalId\":15184,\"journal\":{\"name\":\"Journal of Bioequivalence & Bioavailability\",\"volume\":\"32 1\",\"pages\":\"1-1\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Bioequivalence & Bioavailability\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.35248/0975-0851.21.S2.E002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bioequivalence & Bioavailability","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/0975-0851.21.S2.E002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Bioavailability is alluded to as the degree and rate to which the dynamic medication fixing or dynamic moiety from the medication item is ingested and opens up at the site of medication activity. The general bioavailability as far as the rate and degree of medication ingestion is viewed as prescient of clinical results. In 1984, the United States Food and Drug Administration (FDA) was approved to endorse conventional medication items under the Drug Price Competition and Patent Term Restoration Act dependent on proof of normal bioequivalence in drug assimilation through the direct of bioavailability and bioequivalence considers.