Guideline on reporting the results of population pharmacokinetic analyses

We have adopted this International Scientific Guideline - CHMP/EWP/185990/06

Last updated

15 July 2024

About this guideline

Overseas effective date: 1 January 2008

Categories: Clinical pharmacology and pharmacokinetics | Product-specific bioequivalence

TGA annotations: Nil

Where EU guidelines adopted in Australia include references to EU legislation (including EC Directives and Regulations), the requirements contained in the referenced EU legislation are not applicable to the evaluation of medicines by the TGA.
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