Bioequivalence of oral products and the biopharmaceutics classification system: science, regulation, and public policy.
about
Provisional in-silico biopharmaceutics classification (BCS) to guide oral drug product development.Quantitation of small intestinal permeability during normal human drug absorption.In vitro-in vivo Pharmacokinetic correlation model for quality assurance of antiretroviral drugsBCS Biowaivers: Similarities and Differences Among EMA, FDA, and WHO Requirements.Risk analysis in bioequivalence and biowaiver decisions.The Biopharmaceutics Classification System: subclasses for in vivo predictive dissolution (IPD) methodology and IVIVCRegional-dependent intestinal permeability and BCS classification: elucidation of pH-related complexity in rats using pseudoephedrine.The fraction dose absorbed, in humans, and high jejunal human permeability relationship.
P2860
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P2860
Bioequivalence of oral products and the biopharmaceutics classification system: science, regulation, and public policy.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Bioequivalence of oral product ...... regulation, and public policy.
@ast
Bioequivalence of oral product ...... regulation, and public policy.
@en
type
label
Bioequivalence of oral product ...... regulation, and public policy.
@ast
Bioequivalence of oral product ...... regulation, and public policy.
@en
prefLabel
Bioequivalence of oral product ...... regulation, and public policy.
@ast
Bioequivalence of oral product ...... regulation, and public policy.
@en
P2093
P2860
P356
P1476
Bioequivalence of oral product ...... regulation, and public policy.
@en
P2093
P2860
P304
P356
10.1038/CLPT.2011.109
P407
P577
2011-07-20T00:00:00Z