Guideline on the use of pharmacogenetic methodologies in the pharmacokinetic evaluation of medicinal products

We have adopted this International Scientific Guideline - EMA/CHMP/37646/2009

Last updated

27 August 2024

About this guideline

Overseas effective date: 1 August 2012

Categories: Clinical efficacy and safety | Clinical pharmacology and pharmacokinetics

Multidisciplinary | Pharmacogenomics

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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