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Research Ethics Board (REB)

The primary and clear mandate of the RVHS REB is: The Protection and Safety of the public who are participating in clinical research trials.
 

At RVHS, the REB's clear moral foundation of clinical equipoise requires that people will not be disadvantaged by research participation. The rights, safety and wellbeing of the clinical trial participants are the most important consideration, even above the interests of science. The basic ethical principles of RVHS' REB are to do no harm (non-maleficience), to disclose all facts, to communicate truthfully (veracity) and to conduct valid research.

The RVHS, REB will act in compliance with all laws, policies, standards and guidelines governing human research, which are applicable to a submitted research study including but not limited to the Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans, the World Medical Association Declaration of Helinski, and the Personal Health Information Protection Act.

 

REB Processes

 
REB Policies & Procedures
Additional REB Forms
 

REB Submission Deadlines

 

REB Committee Members

 

Useful Links

 

Research Education

 

 

 

 

 

 

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