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Generic drug product development [[Book] :]International regulatory requirements for bioequivalence / Isadore Kanfer, Leon Shargel.

Von: Kanfer,Isadore.
Mitwirkende(r): Shargel, Leon, 1941- | Kanfer, Isadore.
Materialtyp: materialTypeLabelBuchReihen: Verlag: New York : Informa Healthcare, c2010Beschreibung: xxi, 309 p. : ill. ; 24 cm.ISBN: 9780849377853; 0849377854 (hardcover : alk. paper); 9781420020021 (electronic bk.); 9781420020021.Schlagwörter: 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 | MedicineDDC-Klassifikation: 615.19 | 615.19 Online-Ressourcen: Check for Full Text Access restricted: Dal users only. Print version also available.Zusammenfassung: Discusses the worldwide legislative and regulatory requirements for the registration of generic and multi-source drug products.
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Books Books 6october
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Includes bibliographical references and index.

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

Print version also available.

Mode of access: Internet

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