Frequently Used Services

  • Information on topics such as who may be a Principal Investigator, NYSPI IRB research review requirements, and serious adverse event reporting.

  • CITI training requirements for all persons involved in human subjects research design or conduct of the research.

 
  • The consent form template, MRI Director approval form, serious adverse event form, protocol violation form, conflict of interest form, and many other forms and templates.

 
  • Various resources such as links to Office of Human Research Protections, RFMH, FDA, Nathan Kline Institute, Office of Research Integrity, and CUIMC.

  • Answers to questions regarding PRISM, protocol submission, serious adverse event reporting, CITI training, recruitment materials, and more.