Generic drug product development : international regulatory requirements for bioequivalence /

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Principais autores: Kanfer, Isadore, Shargel, Leon
Formato: Livro
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Endereço do item:https://app.bczm.ufrn.br/home/#/item/161649
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spelling oai:localhost:123456789-2054362022-11-30T16:49:48Z Generic drug product development : international regulatory requirements for bioequivalence / Kanfer, Isadore, Shargel, Leon, Medicamentos - Equivalência terapêutica. Medicamentos genéricos - Legislação. Bioviabilidade. 1 2022-10-11T09:21:49Z 2022-10-11T09:21:49Z c2010. Livro 615.015.11 G326 9780849377853 (enc.). 161649 https://app.bczm.ufrn.br/home/#/item/161649 https://app.bczm.ufrn.br/home/#/item/161649
institution Acervo SISBI
collection SIGAA
topic Medicamentos -
Equivalência terapêutica.
Medicamentos genéricos -
Legislação.
Bioviabilidade.
spellingShingle Medicamentos -
Equivalência terapêutica.
Medicamentos genéricos -
Legislação.
Bioviabilidade.
Kanfer, Isadore,
Shargel, Leon,
Generic drug product development : international regulatory requirements for bioequivalence /
description
format Livro
author Kanfer, Isadore,
Shargel, Leon,
author_facet Kanfer, Isadore,
Shargel, Leon,
author_sort Kanfer, Isadore,
title Generic drug product development : international regulatory requirements for bioequivalence /
title_short Generic drug product development : international regulatory requirements for bioequivalence /
title_full Generic drug product development : international regulatory requirements for bioequivalence /
title_fullStr Generic drug product development : international regulatory requirements for bioequivalence /
title_full_unstemmed Generic drug product development : international regulatory requirements for bioequivalence /
title_sort generic drug product development : international regulatory requirements for bioequivalence /
publishDate 2022
url https://app.bczm.ufrn.br/home/#/item/161649
work_keys_str_mv AT kanferisadore genericdrugproductdevelopmentinternationalregulatoryrequirementsforbioequivalence
AT shargelleon genericdrugproductdevelopmentinternationalregulatoryrequirementsforbioequivalence
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