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Books > Business & Economics > Industry & industrial studies > Manufacturing industries > Pharmaceutical industries

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Generic Drug Product Development - International Regulatory Requirements for Bioequivalence (Hardcover) Loot Price: R5,076
Discovery Miles 50 760
Repayment Terms: R476 pm x 12*
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Generic Drug Product Development - International Regulatory Requirements for Bioequivalence (Hardcover): Isadore Kanfer, Leon...

Generic Drug Product Development - International Regulatory Requirements for Bioequivalence (Hardcover)

Isadore Kanfer, Leon Shargel

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Loot Price R5,076 Discovery Miles 50 760 | Repayment Terms: R476 pm x 12*

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Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of the same quality and are therapeutically equivalent to the brand name alternative. However, many countries have limited resources to inspect and verify the quality of all drug products for sale in their country. This title discusses the worldwide legislative and regulatory requirements for the registration of generic and multi-source drug products.

General

Imprint: Crc Press
Country of origin: United States
Release date: March 2010
First published: February 2010
Editors: Isadore Kanfer • Leon Shargel
Dimensions: 229 x 152 x 23mm (L x W x T)
Format: Hardcover
Pages: 332
ISBN-13: 978-0-8493-7785-3
Categories: Books > Business & Economics > Industry & industrial studies > Manufacturing industries > Pharmaceutical industries
Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry > Pharmaceutical technology
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LSN: 0-8493-7785-4
Barcode: 9780849377853

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