Points to consider on clinical investigation of medicinal products for the treatment of acute stroke

We have adopted this International Scientific Guideline - CPMP/EWP/560/1998

Last updated

19 December 2024

Overseas effective date: 1 April 2002

Categories: Clinical efficacy and safety | Nervous 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.
All documents and other content published by the European Medicines Agency (EMA) on this website are under the copyright and other intellectual property rights ownership of the EMA. Please refer to Legal notice | European Medicines Agency for further information.

Product types

Product regulation