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Generic drug product development[ele...

Kanfer, Isadore.

Generic drug product development[electronic resource] :international regulatory requirements for bioequivalence /

纪录类型:	书目-语言数据,印刷品 : Monograph/item
[NT 15000414] null:	615/.19
[NT 47271] Title/Author:	Generic drug product development : international regulatory requirements for bioequivalence // edited by Isadore Kanfer, Leon Shargel.
[NT 51406] other author:	Kanfer, Isadore.
出版者:	New York : : Informa Healthcare,, c2010.
面页册数:	1 online resource (xxi, 309 p.) : : ill.
标题:	Generic drugs.
标题:	Generic drugs - Law and legislation.
标题:	Drugs, Generic - pharmacokinetics.
标题:	Drugs, Generic - standards.
标题:	Biological Availability.
标题:	Drug Design.
标题:	International Cooperation.
标题:	Legislation, Drug.
标题:	Therapeutic Equivalency.
ISBN:	9781420020021 (electronic bk.)
ISBN:	9786612560972
ISBN:	6612560975
[NT 15000227] null:	Includes bibliographical references and index.
电子资源:	Connect to Informa resource

Generic drug product development[electronic resource] :international regulatory requirements for bioequivalence /
Generic drug product developmentinternational 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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019 $a 647895166
020 $a 9781420020021 (electronic bk.)
020 $a 9786612560972
020 $a 6612560975
020 $z 9780849377853 (hbk.)
020 $z 0849377854 (hbk.)
035 $a (OCoLC)667098785 $z (OCoLC)647895166
035 $a ocn667098785
040 $a IDEBK $b eng $c IDEBK $d E7B $d OCLCQ
050 0 0 $a RS55.2 $b .G454 2010
060 1 0 $a W1 $b DR893B v.201 2010
060 1 0 $a QV 38 $b G3255 2010
082 0 0 $a 615/.19 $2 22
245 0 0 $a Generic drug product development $h [electronic resource] : $b international regulatory requirements for bioequivalence / $c edited by Isadore Kanfer, Leon Shargel.
260 $a New York : $b Informa Healthcare, $c c2010.
300 $a 1 online resource (xxi, 309 p.) : $b ill.
490 1 $a Drugs and the pharmaceutical sciences ; $v 201
504 $a Includes bibliographical references and index.
650 0 $a Generic drugs. $3 437927
650 0 $a Generic drugs $x Law and legislation. $3 437928
650 1 2 $a Drugs, Generic $x pharmacokinetics. $3 437929
650 1 2 $a Drugs, Generic $x standards. $3 437930
650 2 2 $a Biological Availability. $3 437931
650 2 2 $a Drug Design. $3 402272
650 2 2 $a International Cooperation. $3 371644
650 2 2 $a Legislation, Drug. $3 437932
650 2 2 $a Therapeutic Equivalency. $3 437933
700 1 $a Kanfer, Isadore. $3 437925
700 1 $a Shargel, Leon, $d 1941- $3 437926
830 0 $a Drugs and the pharmaceutical sciences ; $v v. 183-184 $3 437650
856 4 $z Connect to Informa resource $u http://informahealthcare.com/action/showBook?doi=10.3109%2F9781420020021

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