Informed consent represents one of the most important ethical aspects of clinical treatments and scientific research involving humans. This article will discuss the key elements of informed consent ...
Providing informed consent is a bedrock of ethical medical practice -- and a physician’s failure to provide proper informed consent is grounds for legal action. But, determining what constitutes ...
Potential research subjects must be accurately informed of what a project involves, and given the opportunity to decide of their own free will whether or not to participate. This process may be brief ...
1don MSN
In drug trials, lack of oversight of research ethics boards could put Canadian patients at risk
New drug approvals by Health Canada are based on the results of clinical trials. But before clinical trials can go ahead, ...
NOTE: The University IRB abides by information regarding the current position of the VHA Office of Research & Development’s (per email from Karen Jeans dated 01/03/14) related to use of Craigslist as ...
When submitting a project through the eIRB system, researchers can request either a waiver of the need for signatures/documentation, or a waiver to alter or omit the entire consent process. In either ...
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