Main Content

Research Documentation and Record Support


Study Start-Up Tool Kit

TitleDescriptionLast Updated
Study Startup ChecklistFor study teams to ensure they have everything necessary in place before starting the study once approved by the IRBJuly 2024
Regulatory Binder GuidanceGuidance and suggested structure of all study and regulatory related documentsJuly 2024
Delegation of Authority LogFor PIs document the roles and responsibilities of study team membersJuly 2024
Training LogRecords any training, such as protocol training or other study-specific training that is provided to study team members but not otherwise documents by a training completion certificateJuly 2024
Participant Eligibility ChecklistDocuments eligibility and ensures that participants meet inclusion criteria requirementsJuly 2024
Screening/Enrollment LogRecords the status of potential participants in a research study, including who was screened for eligibility and who was enrolledJuly 2024
Subject Visit Tracking LogContains all study participants, their relevant study information, as well as tracking information about their completion of project milestonesJuly 2024


Self-Audit Tool- Kit

TitleDescriptionLast Updated
Social Behavioral Self-Audit ChecklistJuly 2024
Clincial Trial and FDA Self Audit ChecklistJuly 2024
Informed Consent ChecklistJuly 2024


Clinical Trial Resources

TitleDescriptionLast Updated
Contents of a 510(k) Premarket NotificationJuly 2024
FDA Regulatory Premarket Pathway and TimelineJuly 2024
How To Set-Up a Study BinderJuly 2024
Investigational Device ExemptionJuly 2024
Premarket ApprovalJuly 2024
What is a Medical DeviceJuly 2024
ClincalTrials.gov Guidance July 2024