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Your Study Reviewed, with
Speed, Quality and Compliance
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Read what our clients have to say about New England IRB
- "You guys are the best – we work with several different IRBs, and hands down, NEIRB is the way to go. I tell all of our Sponsors that as well"-- Clinical Research Coordinator
- "Because of the outstanding and excellent work and relationship I had with your IRB, I recommended to my management to go with your IRB again for this upcoming study. It's no secret that your IRB is an outstanding, professional organization, not to mention the staff at NEIRB are great to work with."-- Clinical Research Manager
- "I have been very pleased with your service and just wanted to say thank you for always being so responsive to my e-mails and so quick to meet our sometimes really tight deadlines."-- CRO Team Leader for Site Activation
- "It's great working with you and the NEIRB staff. You are all so very accommodating, and provide exceptional service."-- Clinical Trials Specialist
- "Among the reasons we appreciate NEIRB are its thoughtful reviews of the proposals we submit, its good communication with our staff, and its knowledge of regulations related to the protection of human subjects involved in research. It is a pleasure working with your team."-- CRO President and CEO
- "It is always a pleasure to work with NEIRB, they have extremely effective and efficient customer service. In comparison with other IRBs I have worked with, NEIRB is absurdly fast.. [and have] significantly better knowledge of federal regulations than I have encountered at other IRBs."-- Assistant Professor of Medicine
New England IRB is a central institutional review board for sponsors, CROs and individual researchers across North America. Our priority is to ensure the safety of human subjects in clinical trials. We are committed to a thorough and ethical IRB review process. Please contact us to discuss your upcoming clinical research study.
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