Sentence examples for through irbs from inspiring English sources

Your argument appears to run: (1) people will be outraged about being experimented on if they're debriefed; (2) managers "chafe" at de-briefing because of the outrage, (3) IRBs would require debriefing; so (4) it's reasonable for companies not to go through IRBs at all [and to conduct the nonconsensual A/B test of 401(k) letters with no debriefing afterward].

The primary means to public assurance in medical research is through IRBs.

Samples for this study were obtained from formalin-fixed, paraffin-embedded tissues from University of Chicago HTRC through IRB-approved protocols.

The formalin-fixed, paraffin-embedded tissues samples were acquired from the archives of the University of Chicago Human Tissue Resource Center (HTRC) available to us through IRB-approved protocols.

The Mississippi State University Institutional Review Board for the Protection of Human Subjects in Research provided approval for the survey instruments via administrative review on January 22 , 2004through IRB Docket #04-005.

Because the experiment involved telling users that their compatibility scores were high when they actually weren't, it probably wouldn't have gotten through many schools' IRBs unless participants were asked for their consent.

De-identified patient samples of primary and metastatic tumors were obtained through an IRB-approved study supported through the tissue procurement facility of the Lineberger Comprehensive Cancer Center.

In this case, Soghoian says the research likely should have gone through the IRB process, but it is unclear if it actually did -- or were aware that they should have.

Remote Monitor Access to Maestro Care (3/12/2019) - This policy describes the process for requesting and granting remote access to medical records for research monitors when access is supported through an IRB-approved research protocol.

To determine whether fascin expression correlated with the clinical course of CRC, we utilized a TMA of colorectal adenocarcinomas for which clinical annotation was available through an IRB-approved database.

The research organisation that conducted this study, RTI Health Solutions, a business unit of RTI International (RTI), holds a Federal-Wide Assurance (FWA #3331 effective until 17 June 2014) from the DHHS Office for Human Research Protections that allows us to review and approve human subjects protocols through our IRB committees.