General:
Administrative Guidelines for Authorship Criteria
Freedom of Information Act (FOIA) Requests
Procedures for Freedom of Information Act (FOIA) Requests
Examples of Freedom of Information Act (FOIA) Request
Open Access to Research Results
Procedures for Open Access to Research Results
Principal Investigator Eligibility
Procedures for Principal Investigator Eligibility
Procedures for Research Conflict of Interest
Significant Financial Interests Limits of Disclosure
Procedures for Research Equipment
Transfer of a Research Project
Transfer of a Research Project – Administrative Procedure
Sponsored Research (Financial Management):
Institutional Policies and Procedures for Sponsored Projects
Administration of Sponsored Projects Policy
Administration of Sponsored Projects Procedures
Cost Sharing, Matching, and In-Kind Contributions on Sponsored Projects
Procedures for Cost Sharing, Matching, and In-Kind Contributions on Sponsored Projects
Cost Transfers on Sponsored Projects
Procedures for Cost Transfers on Sponsored Projects
Charging Direct Costs to Sponsored Projects
Procedures for Charging Direct Costs to Sponsored Projects
Charging Facilities and Administrative (Indirect) Costs to Sponsored Projects
Procedures for Charging Facilities and Administrative (Indirect) Costs to Sponsored Projects
Charging Sponsored Costs Prior to the Budget Period
Procedures for Charging Sponsored Cost Prior to the Budget Period
Delegation of Signature Authority for Sponsored Projects
Procedures for Delegation of Signature Authority for Sponsored Projects
Delinquent Payment and/or Non-Payment of Project Costs by Sponsors
Procedures for Delinquent Payment and/or Non-Payment of Project Costs by Sponsors
Procedures for Effort Reporting
Establishment of a Sponsored Project Account
Procedure for Establishment of a Sponsored Project Account
Procedures for Extending a Sponsored Project
Invoicing of Sponsored Projects
Procedure for Invoicing of Sponsored Projects
Payments to Research Participants Operating Policy
Procedure for Payments to Research Participants
Post Award Changes to Sponsored Projects
Procedures for Post Award Changes to Sponsored Projects
Program Income from Sponsored Projects
Procedures for Program Income from Sponsored Projects
Residual Funds from Sponsored Projects
Procedure for Residual Funds from Sponsored Projects
Guidelines for Residual Funds from Sponsored Projects
Purchasing on Sponsored Projects
Procedures for Purchasing on Sponsored Projects
Procedures for Sponsored Project Closeout
Sponsored Project External Financial Audits
Procedures for Sponsored Project External Financial Audit
Sponsored Project Proposal Review
Procedures for Sponsored Project Proposal Review
Subawards and Subrecipient Monitoring
Procedures for Subawards and Subrecipient Monitoring
Human Studies Research (IRB):
Authority and Independence of the Institutional Review Board
Adverse Event / Unanticipated Problem Reporting and Reviewing
Procedures for Adverse Events / Unanticipated Problems reporting (AE/UP) and Reviewing
Examples of Unanticipated Problems
Change Requests to Human Subject Research
Conduct of Convened Institutional Review Board (IRB) Meetings
Procedures for Conduct of Convened Institutional Review Board (IRB) Meetings
Determination of Human Subject Research
Informed Consent in Human Studies Research
Procedures for Informed Consent in Human Studies Research
Institutional Official (IO) for Human Subject Research
Procedures for Institutional Review of Research
Institutional Review Board Member Conflict of Interest
Procedure for Institutional Review Board Member Conflict of Interest
Guidelines for Institutional Review Board Member Conflict of Interest
Institutional Review Board (IRB) Membership
Provision for a Safe Communication Environment for Research Subjects
Requirements for IRB-Approved Human Subject Research
Research Records, Documentation Retention, Storage, and Access for Human Subject Research
Procedures for Clinical Research Records Documentation
Research Subject Injury/Illness
Review Level – Initial Submissions of Human Subject Research
Review of Humanitarian Use Device (HUD) Application
Roles and Responsibilities of IRB Chair and Vice Chair
Use of Devices in Human Subject Research
Procedures for Significant Risk (SR) / Non-Significant Risk (NSR) Device Determination
Waiver or Alteration of Informed Consent
Clinical Trial Center:
Clinical Trial Medicare Coverage Analysis
Procedures for Clinical Trial Medicare Coverage Analysis