Health and Human Services announced in July a proposal to improve rules protecting human research. The proposed changes can be found in an Advance Notice of Proposed Rulemaking (ANPRM), Human Subjects Research Protections: Enhancing Protections for Research Subjects...
“If it ain’t broke, don’t fix it,” that’s how the old saying goes. That’s not what what Kenneth Getz says about our current state of US human protection IRB system. Getz’ article published in Applied Clinical Trials Online titled...
Barnes & Thornburg LLP and Pearl IRB invite you to join us for a special event focused on the regulatory aspects of clinical research. FEATURED PRESENTATIONS: “Responsibilities of the Site and Clinical Research Principal Investigator: myths and the reality,”...
Gretchen Miller Bowker, COO, Pearl IRB is speaking at the IMDMC regulatory roundtable “Effectively Managing Multi-Center Trials” – REGISTER NOW! Speakers: Jennifer L. Kerr, VP of Operations MED Institute, Inc. Jenna Sallee, Executive Director...
Come join us at an event hosted by the Indianapolis Section of ASQ for their January 2011 Dinner Meeting. Gretchen Bowker, COO of Pearl IRB will present “IRBs Past and Future” Date: Tuesday, 11 Jan 2011 5:30 PM – 7:30 PM – EasternTime...
Goal of Barack’s Memo??? Recently our President, Barack Obama, issued a memo asking Dr. Amy Guttmann, chair, Presidential Commission for the Study of Bioethical Issues, for a review of human subjects protection....