Guideline on the clinical development of medicinal products for the treatment of cystic fibrosis

We have adopted this International Scientific Guideline - EMEA/CHMP/EWP/9147/2008-corr.

Last updated

3 June 2024

About this guideline

Overseas effective date: 30 April 2010

Categories: Clinical efficacy and safety | Respiratory system

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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