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CRC Press Generic Drug Product Development: International Regulatory Requirements for Bioequivalence: 201 (Drugs and the Pharmaceutical Sciences)

Name: Generic Drug Product Development: International Regulatory Requirements for Bioequivalence: 201 (Drugs and the Pharmaceutical Sciences)
Brand: CRC Press

Pharmacology

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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.

Product Specifications

Brand: CRC Press
Format: Hardcover
ASIN: 0849377854
Category: Books > Subjects > Health, Family & Lifestyle > Medical & Healthcare Practitioners > Other Branches of Medicine > Pharmacology
Domain: Amazon UK
Release Date: 27 September 2019
Listed Since: 02 January 2007

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CRC Press Generic Drug Product Development: International Regulatory Requirements for Bioequivalence: 201 (Drugs and the Pharmaceutical Sciences)

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