Generic Drug Product Development-regulatory Issues

Because of the 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 they are of the same quality and are the therapeutic 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.Shargel, Leon is the author of 'Generic Drug Product Development-regulatory Issues ', published 2007 under ISBN 9780849377853 and ISBN 0849377854.