steady workflow. e Commissioned an audit of 10% of all active human subject trials for compliance to good clinical practice (GCP). Collaborated with Institutional Review Board (IRB) Chair when remediation was necessary. Sat on the IRB. e Invited by Dr. Barry Coller, Chairman of Medicine to join the Patient Oriented Researc

lar response. and the ability to complete the study packet in more than one sitting. All information was collected via participant self-report, and Institutional Review Board (IRS) approval was given by the University of Medicine and Dentistry of New Jersey. Participants were allowed to save responses online and return t

eriod after infants' discharge from the NICU and throughout the 2 year project period. Informed, written consent will be obtained in accordance with Institutional Review Board guidelines at each of the hospitals — Massachusetts General Hospital, Boston Children's Hospital, and Beth Israel Deaconess Medical Center - where

tiously so we can start collecting musciality data via phone and our iMABS website? Because you collectively represent all the key components of an Institutional Review Board appropriate to review our protocol - i.e., lay, medical, scientific, and musical perspective- and all of you are members of The Institute's Executiv