Jul 27, 2017 | Featured News Article, Regulatory Updates
On July 24, 2017 the FDA announced a new guidance, effective immediately, which will have significant impacts on industry, IRBs, and investigators. In short, the guidance is being issued to permit IRBs to waive or alter informed consent for minimal risk clinical...
Jun 28, 2017 | Common Rule Updates, Featured News Article
We are happy to help you and your organization as you prepare for the “Common Rule” changes. Download the following electronic copies so that you may pass them along to your institution and/or colleagues: Implementing the Revised Common Rule – 10...
Jan 19, 2017 | Regulations
As you likely have heard the final revisions to the Common Rule were released yesterday, to be published in the Federal Register today, January 19. We are happy to provide you with a summary of the changes. Please note that the new administration still has the ability...
Jun 21, 2016 | Hot Topics, Uncategorized
The NIH has released its final policy on the use of central IRBs for multi-site research. Starting May 2017, in multi-site studies in the United States involving non-exempt human subjects research funded by the National Institutes of Health (NIH), research...
Aug 17, 2013 | Did You Know?
HRP Consulting Group has evaluated numerous institutions’ research ethics programs and has determined that the majority of the best institutions have one thing in common: those institutions have all, if not most, of their research ethics program staff CIP or...
