Isadore Kanfer,
Leon Shargel
Generic Drug Product Development
International Regulatory Requirements for Bioequivalence
Paperback Engels 2019 9780367384371Levertijd ± 8 werkdagen
Gratis verzonden
Samenvatting
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.
Specificaties
ISBN13:9780367384371
Taal:Engels
Bindwijze:Paperback
Aantal pagina's:332
Uitgever:Taylor & Francis Ltd
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Inhoudsopgave
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.
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