The REB is comprised of 15 – 20 scientific and non-scientific members including physicians, clinical staff, non-affiliated community members/lawyers, and individuals knowledgeable in ethics and privacy relevant to research involving humans.
The SRHC Research Ethics Board is organized and operates in accordance with the Tri-Council Policy Statement on Ethical Conduct of Research Involving Humans (TCPS2 2014); Canadian General Standards Board (CGSB) 191.1-2013; Clinical Trials Ontario (CTO) REB Qualification Standards, the International Conference on Harmonisation (ICH) Good Clinical Practice Guidelines (GCP); Part C, Division 5 of the Food and Drug Regulations of Canada; Part 4 of the Natural Health Product Regulations; Medical Devices Regulations, and the provisions within the Ontario Personal Health Information Protection Act (PHIPA) and all other applicable laws and regulations. The SRHC REB is registered with the U.S. Department of Health and Human Services (DHHS) Office for Human Research Protection (OHRP).
If you are interested in volunteering as a REB member, please contact the REB Administrator
REB Membership Lists (PDF Format)