Download the template(s) of your choice. The template documents open as Word files; save as a Word file to begin drafting your protocol. All instructions in the template are highlighted in blue.

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 ...

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 involvement in human subject ...

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 ...

Each School and Faculty have developed a suite of study document templates based on key ethical issues. Applicants are encouraged to use the templates when developing their research ethics application ...

If so, then you will need to have your research reviewed by the William & Mary Institutional Review Board (IRB) before you begin your research involving human subjects, so that we're sure that your ...