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Generic drug product development[ele...
~
Kanfer, Isadore.
Generic drug product development[electronic resource] :international regulatory requirements for bioequivalence /
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
杜威分類號:
615/.19
書名/作者:
Generic drug product development : international regulatory requirements for bioequivalence // edited by Isadore Kanfer, Leon Shargel.
其他作者:
Kanfer, Isadore.
出版者:
New York : : Informa Healthcare,, c2010.
面頁冊數:
1 online resource (xxi, 309 p.) : : ill.
標題:
Generic drugs.
標題:
Generic drugs - Law and legislation.
標題:
Drugs, Generic - pharmacokinetics.
標題:
Drugs, Generic - standards.
標題:
Biological Availability.
標題:
Drug Design.
標題:
International Cooperation.
標題:
Legislation, Drug.
標題:
Therapeutic Equivalency.
ISBN:
9781420020021 (electronic bk.)
ISBN:
9786612560972
ISBN:
6612560975
書目註:
Includes bibliographical references and index.
電子資源:
Connect to Informa resource
Generic drug product development[electronic resource] :international regulatory requirements for bioequivalence /
Generic drug product development
international regulatory requirements for bioequivalence /[electronic resource] :edited by Isadore Kanfer, Leon Shargel. - New York :Informa Healthcare,c2010. - 1 online resource (xxi, 309 p.) :ill. - Drugs and the pharmaceutical sciences ;201. - Drugs and the pharmaceutical sciences ;v. 183-184.
Includes bibliographical references and index.
ISBN: 9781420020021 (electronic bk.)Subjects--Topical Terms:
437927
Generic drugs.
LC Class. No.: RS55.2 / .G454 2010
Dewey Class. No.: 615/.19
National Library of Medicine Call No.: W1 / DR893B v.201 2010
Generic drug product development[electronic resource] :international regulatory requirements for bioequivalence /
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international regulatory requirements for bioequivalence /
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edited by Isadore Kanfer, Leon Shargel.
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http://informahealthcare.com/action/showBook?doi=10.3109%2F9781420020021
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