The new European Medicines Agency guideline on the investigation of bioequivalence.
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Pharmacokinetics and pharmacodynamics of tiotropium solution and tiotropium powder in chronic obstructive pulmonary diseaseImplementation of a reference-scaled average bioequivalence approach for highly variable generic drug products by the US Food and Drug Administration.Current regulatory approaches of bioequivalence testing.Effect of food on the bioavailability of palbociclib.Differentiating biosimilarity and comparability in biotherapeutics.Utility of Pilot Studies for Predicting Ratios and Intrasubject Variability in High-Variability Drugs.Effect of Truncating AUC at 12, 24 and 48 hr When Evaluating the Bioequivalence of Drugs with a Long Half-Life.Dissolution studies of physical mixtures of indomethacin with alpha- and gamma-cyclodextrins.Bioavailability of Sandimmun® versus Sandimmun Neoral®: a meta-analysis of published studies.
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P2860
The new European Medicines Agency guideline on the investigation of bioequivalence.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 07 January 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
The new European Medicines Agency guideline on the investigation of bioequivalence.
@en
The new European Medicines Agency guideline on the investigation of bioequivalence.
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type
label
The new European Medicines Agency guideline on the investigation of bioequivalence.
@en
The new European Medicines Agency guideline on the investigation of bioequivalence.
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prefLabel
The new European Medicines Agency guideline on the investigation of bioequivalence.
@en
The new European Medicines Agency guideline on the investigation of bioequivalence.
@nl
P1476
The new European Medicines Agency guideline on the investigation of bioequivalence
@en
P2093
Maria do Rosário Lobato
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P356
10.1111/J.1742-7843.2009.00518.X
P50
P577
2010-01-07T00:00:00Z