Abstracted Scientific Content

Published in:
Volume 10 / Year 2021 / Issue 3

An IPRP survey of the regulatory requirements for the waiver of in vivo bioequivalence studies of generic medicinal products in certain dosage forms

Author(s): ,
Page: 146-8

Submitted: 14 May 2021; Revised: 14 May 2021; Accepted: 3 June 2021; Published online first: 10 June 2021 Medicines regulatory authorities aim to address rising healthcare costs and promote access… Read More »

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