Author Archives: admin

October 2011 – The CAREB Board of Directors recently filed comments to the Department of Health and Human Services (HHS) in response to an Advanced Notice of Proposed Rulemaking (ANPRM) entitled Human Subjects Research Protections: Enhancing Protections for Research Subjects and Reducing Burden, Delay, and Ambiguity for Investigators (Notice Number HHS-OPHS-2011-0005), published in the July 26, 2011 Federal Register (76 […]

September 2011 – The CAREB Board of Directors filed comments in response to the Tri-Agency’s proposed framework on the Responsible Conduct of Research (RCR). While it was agreed that the framework is well written, several aspects of the document could be strengthened in terms of scope and process. File: Final Comments Tri-Agency RCR Framework Sept 2011

July 2010 – CAREB issued their first guidance document Reporting of Unanticipated Problems including Adverse Events to Research Ethics Boards in Canada. This document is intended to assist the research ethics community in Canada in standardizing the reporting of unanticipated problems, including certain adverse events, and should be viewed as a recommendation only. File: CAREB Guidance – AE Reporting […]