Download the Pending IRB Approval Template & Instructions via WUSTL Box.
Category: Forms and Templates
RCR Continuing Education Submission Form
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Transparency of Foreign Connections
Some funding agencies, especially the DOE and NASA, may require information at the time of application on Transparency of Foreign Connections. WashU has a Transparency of Foreign Connections – Institutional Responses document available for download from Box (WUSTL Key required).
DCM Safety Recommendation and Near Miss Form
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Animal Facility Visitor Waiver
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NSF Policy for Safe and Inclusive Working Environments for Off-Campus or Off-Site Research
Effective January 30, 2023, NSF instituted a requirement for Safe and Inclusive Working Environments for Off-Campus or Off-Site Research. NSF PIs are responsible for:
Award Setup Form (Financial Services Forms)
Financial Services Forms
Essential Regulatory Documentation
Purpose Essential Documents are those documents which individually and collectively permit evaluation of the conduct of a trial and the quality of the data produced. These documents serve to demonstrate the compliance of the investigator, sponsor, and monitor with the standards of Good Clinical Practice and all applicable regulatory requirements. Best Practice Considerations Templates Monitoring/Auditing […]
Documentation of Study Visit Interventions/Observations
Purpose The purpose of source documentation is to reconstruct the research study as it happened. It should allow for data to be confirmed, validated, and support the fundamental principle of protecting the participant’s rights, safety and well-being. These templates are intended to assist in documenting study procedures, interventions, observations, etc. Below are several examples that […]
Documentation of Informed Consent
Purpose These templates are intended to assist in documenting the consent discussion and process with potential participants. There are many ways to document the informed consent process. Below are several examples that can be customized to meet your specific study needs/requirements (study populations, optional items etc.). Best Practice Considerations Documentation of the consent/assent process should […]