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Einfache Ansicht MARC ISBD

Kanfer,Isadore

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 .

Includes bibliographical references and index.

Discusses the worldwide legislative and regulatory requirements for the registration of generic and multi-source drug products.




Mode of access: Internet

ISBN: 9780849377853 0849377854 (hardcover : alk. paper) 9781420020021 (electronic bk.) 9781420020021

Subjects--Topical Terms:
Generic drugs.
Generic drugs--Law and legislation.
Drugs, Generic--pharmacokinetics.
Drugs, Generic--standards.
Biological Availability.
Drug Design.
International Cooperation.
Legislation, Drug.
Therapeutic Equivalency.
Biological availability.
Drug design.
Drugs, Generic -- Pharmacokinetics.
Drugs, Generic -- Standards.
Generic drugs -- Law and legislation.
Generic drugs.
International cooperation.
Legislation, drug.
Therapeutic equivalency.
Pharmacy.
Medicine.

LC Class. No.: RS55.2 / .G454 2010 RS55.2 .G454 2010

Dewey Class. No.: 615.19 615.19

National Library of Medicine Call No.: W1 / K G QV 38 / G3255 2010