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Generic Drug Product Development on Hardback
Generic Drug Product Development on Hardback
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Generic Drug Product Development

International Regulatory Requirements for Bioequivalence
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Hardback
$569.00
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Description

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.

Author Biography:

Isadore Kanfer, Leon Shargel
Release date NZ
March 25th, 2010
Audience
  • Professional & Vocational
Contributors
  • Edited by Isadore Kanfer
  • Edited by Leon Shargel
Pages
336
Dimensions
152x229x23
ISBN-13
9780849377853
Product ID
2788766

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