All clinical studies^[i] supported by TDR must be carried out according to International Conference on Harmonisation (ICH) / WHO Good Clinical Practice standards, regulatory authorities requirements, and TDR Standard Operating Procedures (SOPs).

If your proposed research involves clinical trials or studies,

Read the TDR Standard Operating Procedures for Clinical Investigators (TDR/TDP/SOP/99.1) available in PDF* (103Kb), or on request from TDR

*PDF files can be read using Adobe Acrobat Reader