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Examples
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Bioequivalence tests are conducted on healthy people, not those who need the medication, and each gets just a single dose, so there is no chance to work up to 300 mg slowly, as actual patients are advised to do.
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A confirmatory Phase 1 Bioequivalence Study followed by a Safety Study, are expected to lead to a New Drug Application by late 2013 or early 2014.
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Bioequivalence are measures that assure that manufacturers are producing a quality product that is in every way comparable to its trade name equivalent.
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Bioequivalence are measures that assure that manufacturers are producing a quality product that is in every way comparable to its trade name equivalent.
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Bioequivalence studies show that Dynapar AQ 1ml injection offers higher bioavailability compared to conventional 3ml Diclofenac injection.
DWS Full News Feed 2010
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Bioequivalence and comparable toxicity of ADVENTRX Pharmaceuticals 'ANX-514 and Taxotere affirmed
THE MEDICAL NEWS Editors 2010
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Bioequivalence and comparable toxicity of ADVENTRX Pharmaceuticals 'ANX-514 and Taxotere affirmed
THE MEDICAL NEWS Editors 2010
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Bioequivalence studies show that Dynapar AQ 1ml injection offers higher bioavailability compared to conventional 3ml Diclofenac injection.
DWS Full News Feed pillscribe 2010
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• Bioequivalence: What patent lawyers need to know (patent track);
Patent Docs 2009
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The Clinical Pharmacology Unit carries out Bioequivalence studies meeting international regulatory requirements like USFDA (USA), ANVISA (Brazil), AFSSAPS (France) and WHO (World Health Organization, Geneva) and has successfully cleared their audits.
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