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 ...

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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 ...

735. Protocol Deviations Updated June 10, 2024 A protocol deviation or violation is any departure from the study procedures or treatment plans as specified in the IRB-approved protocol. Protocol ...

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 ...

BOSTON, MA--(Marketwired - Jan 14, 2016) - Research sponsors implement at least one substantial global amendment for nearly 60% of all clinical trial protocols, substantially reducing the number ...

Human research for student theses and dissertations always requires prior IRB approval. Data collected before approval is obtained cannot be used for research. Who can be the Principal Investigator of ...

Increased Efficiency: eProtocol automation can help clinical research organizations to reduce the time and resources required for protocol development. By automating repetitive tasks, such as creating ...