If you are a Geisel/TDI student interested in performing your own clinical study at DH, there are many more steps you must take in order to complete this process. The document below details the personal training (and links to that training) that needs to be completed (Citi, Consent, Ereg) but also the requirements for IRB, RIDGE (data management and security) and Oncore/Clinical Trials Office. All of these regulatory steps must be completed (in addition to writing the protocol, obtaining grant funding, etc) before you can begin performing your own trial. These steps are required by DH even if you are performing a smaller study such as a retrospective chart review. Please reach out to Dr. Gardner with questions.