Generic pharmaceuticals, regulatory aspects, bioequivalence investigation, and perception
Sign Up to like & getrecommendations! Published in 2024 at "Expert Opinion on Drug Safety"
DOI: 10.1080/14740338.2024.2305709
Abstract: ABSTRACT Introduction The objective and significance of the topic is to draw attention toward regulatory aspects (and pharmacopoeias) for bioequivalence investigation, and perception for generic pharmaceuticals, especially their stereoselective bioequivalence evaluation for understanding the performance… read more here.
Keywords: bioequivalence investigation; regulatory aspects; investigation perception; bioequivalence ... See more keywords