An Institutional Review Board (IRB) is a federally mandated organization of scientific and non-scientific persons. Our charge is to review research studies involving human subjects to ensure subject safety and welfare and to ensure that any research study under our jurisdiction is in compliance with federal, state, and institutional regulations. In addition, the IRB office staff provide administrative support for the institutional Scientific Review Committee (SRC).
The Tufts Medical Center and Tufts University Health Sciences (TUHS) IRB has jurisdiction over the following:
The Tufts Medical Center and TUHS IRB is divided into two IRBs, IRB-Red and IRB-Blue. Each IRB meets once a month. Each IRB is constituted and equipped to review any type of research study involving human subjects.
The IRB office is available to faculty, staff, and students conducting human subjects research at Tufts Medical Center and Tufts University as a resource to provide guidance and assistance with protocol and informed consent form (ICF) development, research education and training, and information and direction on federal research-related regulations and guidance, state laws, and institutional policies.
The IRB office is available to assist investigators with the monitoring of research, preparation for site visits (for example, sponsor or FDA inspections), and to orient new researchers to human subject protection matters.
The IRB office staff is also available to help provide orientation to new study coordinators, and to provide ongoing guidance to study coordinators.