References
- E3 Implementation Working Group ICH E3 Guideline: Structure and Content of Clinical Study Reports Questions & Answers (R1). International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use; 6 July 2012 [cited 2012 Sep 1]. Available from: http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Efficacy/E3/E3_QAs_R1_Step4.pdf
- ICH harmonised Tripartite Guideline: Structure and Content of Clinical Study Reports, E3. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use; Step 4, 30 November 1995 [cited 2012 Sep 1]. Available from: http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Efficacy/E3/E3_Guideline.pdf.