Generic Drug Product Development

International Regulatory Requirements for Bioequivalence
1. Auflage 2010
ISBN: 978-0-8493-7785-3
Verlag: CRC Press

Buch, Englisch, 336 Seiten, Format (B × H): 157 mm x 235 mm, Gewicht: 638 g

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.

Zielgruppe

Academic and Professional Practice & Development

Autoren/Hrsg.

Kanfer, Isadore

Shargel, Leon

Fachgebiete

• Technische Wissenschaften Verfahrenstechnik | Chemieingenieurwesen | Biotechnologie Pharmazeutische Technologie
• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizinische Fachgebiete Pharmakologie, Toxikologie

Inhaltsverzeichnis

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.

Über Autor(innen)

Isadore Kanfer, Leon Shargel