In order to address the specific details and regulatory requirements present in a retrospective medical chart review, the UB IRB recently created a new Protocol template: the HRP-503R. In order to ...

List of terms commonly used in clinical trial research. Glossary of Medical Terms in Lay Language Helpful list of medical terms described in lay language. Sample Study Startup Checklist Use this ...

Preparing & Submitting a Protocol Follow the step-by-step instructions below to successfully prepare and submit a protocol to the IRB. Instructions below include information about single IRBs, student ...

The Principal Investigator (PI) is responsible for reviewing this policy and complying with its requirements. Specifically, the PI will: You may use the protocol template to record your information ...

Tricks of the Trade: Plan early to submit your new protocol submission to give the CWRU IRB time to review, process and approve it. Selecting the correct type of protocol template to match your ...

When using single IRB review, it is important to ensure that the protocol includes a detailed recruitment plan, consent process, and data and safety monitoring plans. The investigators should also ...

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Maintaining & Closing a Protocol Maintaining & Closing a Protocol Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include ...

Full Board (level 3) reviewed research activities require review through a convened meeting and a majority vote of approval by the IRB. Occurs during Expedited (level 2) review, an IRB member calls ...

Investigators must use Cayuse to electronically submit new research studies for review and approval, course approvals, continuing research requests, amendments to approved research studies, and ...