Sub menu

 
 

Guideline on the clinical development of medicinal products for the treatment of HIV infection

We have adopted this International Scientific Guideline - EMEA/CPMP/EWP/633/02 Rev. 3 

Last updated

About this guideline

Overseas effective date: 1 January 2017

Replaces: EMEA/CPMP/EWP/633/02 Revision 2 Guideline on the Clinical Development of Medicinal Products for the Treatment of HIV Infection (adopted by TGA 15 July 2009)

Categories: Clinical efficacy and safety | Anti-infectives for systemic use

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.

For more information see International scientific guidelines adopted in Australia.

Topics

Help us improve the Therapeutic Goods Administration site