Health Sciences IRB
New Researchers and Research Coordinators: Request a Virtual Orientation with the IRB Staff!
Announcements
Check Out the Tufts Health Sciences IRB Newsletter!
Have you read the Winter IRB Newsletter yet? Don’t miss this opportunity to learn helpful tips and reminders, updates on recent changes to the regulations, and IRB form updates!
As the next step in our goal to create one Tufts Medicine-wide IRB, the Lowell General Hospital Clinical Research Review Committee has been integrated with the Tufts Health Sciences IRB (Tufts HS IRB) to form one IRB. Tufts Health Sciences IRB now serves as the IRB for Lowell General as well as MelroseWakefield Healthcare. Please note that our health system is able to support specific types of research activity at Lowell General and MelroseWakefield at this time. For more details, please see the full announcement.
About
The Tufts Health Sciences Institutional Review Board (HS IRB) is federally mandated to review, monitor and approve biomedical and social, behavioral, and educational research. Our goal is to ensure that any research study under Tufts Health Sciences IRB jurisdiction is in compliance with federal, state, and institutional regulations. The Tufts Health Sciences IRB upholds the highest standards, ensuring compliance with ethical principles and regulatory requirements, while serving the Tufts Medicine and Tufts University Health Sciences community of scholars and administering a thorough review in a timely and efficient manner.
Scope & Authority
The Tufts Health Sciences IRB serves Tufts Medicine and Tufts University Health Sciences and has jurisdiction over the following:
- Tufts Medical Center
- Tufts Children's Hospital
- MelroseWakefield Healthcare (MelroseWakefield Hospital and Lawrence Memorial Hospital)
- Lowell General Hospital
- New England Eye Center
- Tufts University School of Medicine (TUSM)
- Tufts University School of Dental Medicine (TUSDM)
- Cummings School of Veterinary Medicine
- Jean Mayer U.S. Department of Agriculture Human Nutrition Research Center on Aging at Tufts University (HNRCA)
- Friedman School of Nutrition
IRBs
The Tufts Health Sciences 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.
Faculty, Staff and Students
The IRB office is available to faculty, staff, and students conducting human subjects research at Tufts Medicine and Tufts University Health Sciences 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.
Investigators
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.
Study Coordinators
The IRB office staff is also available to help provide orientation to new study coordinators, and to provide ongoing guidance to study coordinators.