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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: R5,395

Discovery Miles 53 950

Repayment Terms: R506 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 R5,395 Discovery Miles 53 950 | Repayment Terms: R506 pm x 12*

Expected to ship within 12 - 19 working days

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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 Promotions
LSN:	0-8493-7785-4
Barcode:	9780849377853