Generic Drug Product Development Generic Drug Product Development

Generic Drug Product Development

Bioequivalence Issues

    • $244.99
    • $244.99

Publisher Description

The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counterpart. Generic pharmaceutical products must be approved as therapeutic equivalents to the brand name alternative in order to be interchangeable. The demonstration of bioequivalence is an important comp

GENRE
Professional & Technical
RELEASED
2007
November 15
LANGUAGE
EN
English
LENGTH
288
Pages
PUBLISHER
CRC Press
SELLER
Taylor & Francis Group
SIZE
6.9
MB
Bioequivalence Requirements in Various Global Jurisdictions Bioequivalence Requirements in Various Global Jurisdictions
2025
Generic Drug Product Development Generic Drug Product Development
2016
Bioequivalence Requirements in Various Global Jurisdictions Bioequivalence Requirements in Various Global Jurisdictions
2017