Generic Drug Product Development - International Regulatory Requirements for Bioequivalence

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.

List of contents

Introduction. Australasia. Brazil. Canada. The European Union. India. Japan. South Africa. South America and Pan American Health Organization. Taiwan. Turkey. United States of America. The World Health Organization.

About the author

Isadore Kanfer, Leon Shargel

Product details

• Authors: Isadore Kanfer, Isadore Kanfer Kanfer, Isadore Shargel Kanfer, Leon Shargel
• Assisted by: Isadore Kanfer (Editor), Kanfer Isadore (Editor), Leon Shargel (Editor)
• Publisher: Taylor & Francis Ltd.
• Languages: English
• Product format: Paperback / Softback
• Released: 31.08.2019
• EAN: 9780367384371
• ISBN: 978-0-367-38437-1
• No. of pages: 332
• Subjects: Natural sciences, medicine, IT, technology > Medicine > Non-clinical medicine; Social sciences, law, business > Business > Individual industrial sectors, branches; SCIENCE / Chemistry / General, MEDICAL / Pharmacology, Pharmacology, Pharmaceutical technology, Manufacturing industries, Pharmaceutical industries, Pharmaceutical chemistry and technology