Generic Drug Product Development : International Regulatory Requirements for Bioequivalence

Name: Generic Drug Product Development
Brand: Taylor & Francis Ltd
SKU: 9780367384371
Price: 12800 KES
Availability: OutOfStock
ISBN: 9780367384371

Book Details

Format Paperback / softback

ISBN-10 036738437X

ISBN-13 9780367384371

Publisher Taylor & Francis Ltd

Imprint CRC Press

Country of Manufacture GB

Country of Publication GB

Publication Date Sep 5th, 2019

Print length 332 Pages

Weight 500 grams

Dimensions 15.20 x 22.90 x 2.00 cms

Product Classification: Manufacturing industries Pharmaceutical industries Pharmacology Pharmacology Pharmaceutical chemistry and technology Pharmaceutical technology

KSh 12,800.00

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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.

Get Generic Drug Product Development by Isadore Kanfer at the best price and quality guaranteed only at Werezi Africa's largest book ecommerce store. The book was published by Taylor & Francis Ltd and it has 332 pages.