Buch, Englisch, 345 Seiten, Previously published in hardcover, Format (B × H): 155 mm x 235 mm, Gewicht: 540 g
Buch, Englisch, 345 Seiten, Previously published in hardcover, Format (B × H): 155 mm x 235 mm, Gewicht: 540 g
Reihe: AAPS Advances in the Pharmaceutical Sciences Series
ISBN: 978-3-319-88542-1
Verlag: Springer International Publishing
Although the Bioequivalence (BE) requirements in many global jurisdictions have much in common, differences in certain approaches and requirements such as definitions and terms, choice of comparator (reference) product, acceptance criteria, fasted and fed studies, single and multi-dose studies, biowaivers and products not intended for absorption into the systemic circulation (locally acting medicines and dosage forms), amongst others, provide food for thought that standardisation should be a high priority objective in order to result in a harmonized international process for the market approval of products using BE. An important objective of Bioequivalence Requirements in Various Global Jurisdictions is to attempt to gather the various BE requirements used in different global jurisdictions to provide a single source of relevant information. This information from, Brazil, Canada, China, European Union, India, Japan, MENA, Russia South Africa, the
USA and WHO will be of value to drug manufacturers, regulatory agencies, pharmaceutical scientists and related health organizations and governments around the world in the quest to harmonize regulatory requirements for the market approval of generic products.Zielgruppe
Research
Autoren/Hrsg.
Fachgebiete
Weitere Infos & Material
Brazil.- Canada.- China.- The European Union.- India.- Bioequivalence Studies in Japan.- Middle East and North Africa (MENA) Bioequivalence Requirements.- Russia.- South Africa.- The United States of America.- World Health Organization (WHO).