You may require this guidance note if you work in a medical field where clinical trials are performed.
This guidance note is an internationally accepted standard. The note outlines an international ethical and scientific quality standard for the designing, conducting, recording and reporting of clinical trials. Please note that these standards may be overridden by national legal requirements and the requirements of individual regulatory agencies.
Please consult the Contact Officer for more information and to ascertain the level of compliance (if any) that may be required.