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Forms: Regulatory

FDA 1572: Statement of Investigator Form (Pre-filled)
The primarly use is to identify qualified investigators and as experts to particpate in clinical investigations at the NCI.
CTEP IDF: Supplemental Investigator Data Form (Pre-filled)
Collection of this information serves two purposes. The first is to identify qualified investigators and associates to participate in the clinical investigations at NCI. The second purpose is to ensure that investigational agents are under the control a
MIAP - MICHR IND/IDE Investigator Assistance Program
The MIAP's primary focus is to offer regulatory assistance to sponsor-investigators of a new drug, biologic or medical device to ensure clinical research.excellence and regulatory compliance
CTEP AdEERS (web submission)
NCI's web-based system for submitting expedited reports for serious and/or unexpected events forwarded to designated recipients and the NCI for all trials using a NCI-sponsored investigational agent.

Forms: Study

Transfer of Study Participant Between Investigational Sites
This form should be completed when transferring a UM study participant to another institutional site; or when a study participant from another site is transferring to a UM investigator.
Clinical Research Team (CRT) - Protocol Peer Review Form
This form should be completed by chair assigned reviewers when CRTs are reviewing protocols prior to PRC submission.
Clinical Research Team (CRT) - CTSU Feasibility Review Form
This form should be completed by CTSU personnel when CRTs are reviewing protocols prior to PRC submission.

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