The University IRB follows federal regulations and guidance for reporting unanticipated problems involving risks to participants or others (Unanticipated Problems), serious or continuing noncompliance ...

The University at Buffalo Clinical and Translational Science Institute (CTSI) is launching a new section in its two-times-per-month Translational Spotlight newsletter, one designed to share the latest ...

Research with human participants in countries outside the United States must comply ethical standards. Additional considerations may be required depending on the country of research. Furthermore, ...

The full Case Western Reserve University Institutional Review Board (IRB) meets once per month. Meeting dates and deadlines can be found here. An investigator should expect a protocol requiring full ...

Minutes of IRB meetings will be prepared in sufficient detail to demonstrate that IRB meetings were convened with a quorum of members and IRB deliberations reflecting appropriate regulatory and legal ...

After releasing a report requested nearly three years ago, Sen. Elizabeth Warren said the Food and Drug Administration (FDA) and HHS “should clean up the industry to keep patients safe.”[1] The ...

Faculty in the process of transitioning to another institution or retiring from Purdue need to be aware that their active human subject protocols must be appropriately closed or transferred to a new ...

The IRB is required to review allegations of misconduct and to take action to protect human subjects. Please contact the IRB Chair or submit a Participant Complaint Form if you have a concern about a ...

Federal regulations mandate that information given to potential research participants or their representatives be in a language that they can understand. Translation of research documents, thus, is ...

Business-to-business market research services provider Internet Research Bureau (IRB) has formed a healthcare professionals ...

All human research studies conducted by personnel affiliated with the University at Buffalo must be submitted to the Institutional Review Board (IRB) for review and approval. Research cannot commence ...