Kanfer,Isadore <br/><br/>
Generic drug product development  International regulatory requirements for bioequivalence /  [[Book] :] 
Isadore Kanfer, Leon Shargel. 
 - New York :  Informa Healthcare,  c2010. 
 - xxi, 309 p. :  ill. ;  24 cm. 
 - Drugs and the pharmaceutical sciences ;  201 .
<br/><br/>Includes bibliographical references and index. 
<br/><br/> Discusses the worldwide legislative and regulatory requirements for the registration of generic and multi-source drug products. 
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<br/><br/><br/>Mode of access: Internet 
<br/><br/><label>ISBN: </label>9780849377853 0849377854 (hardcover : alk. paper) 9781420020021 (electronic bk.) 9781420020021 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Generic drugs.<br/>Generic drugs--Law and legislation.<br/>Drugs, Generic--pharmacokinetics.<br/>Drugs, Generic--standards.<br/>Biological Availability.<br/>Drug Design.<br/>International Cooperation.<br/>Legislation, Drug.<br/>Therapeutic Equivalency.<br/>Biological availability.<br/>Drug design.<br/>Drugs, Generic -- Pharmacokinetics.<br/>Drugs, Generic -- Standards.<br/>Generic drugs -- Law and legislation.<br/>Generic drugs.<br/>International cooperation.<br/>Legislation, drug.<br/>Therapeutic equivalency.<br/>Pharmacy.<br/>Medicine.
<br/><br/><label>LC Class. No.: </label>RS55.2  / .G454 2010 RS55.2 .G454 2010 
<br/><br/><label>Dewey Class. No.: </label>615.19 615.19 
<br/><br/><label>National Library of Medicine Call No.: </label>W1  / K G QV 38  / G3255 2010