You must use Chrome when accessing SUBS. Other browsers are not supported. System Access To request access email firstname.lastname@example.org requesting access to the subs system and copy your manager. Security access is no longer based on department. All department users have access to all sub-agreement information. Training & Resources What’s New with New SUBS? See this info sheet […]
Determine Available Animal Balance
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Monitoring Guidance and FAQs
See also: COVID-19 Monitoring Guidance Approved: June 24, 2020Administratively Revised: August 20, 2021 Purpose and Applicability Guidance Centralized Monitoring or Remote Monitoring On-Site Monitoring Monitoring of Multi-Centered PI-Initiated Trials Frequently Asked Questions (FAQs) Resources I. Purpose and Applicability Monitoring procedures have evolved in recent years due to advancements in technology. Washington University in St. Louis is […]
Internally monitoring and self-auditing human research studies is a valuable way for researchers to ensure that participants’ rights, safety and welfare are protected and that the research is conducted in accordance with the approved research plan and documented according to best practices. The Key Elements for Monitoring Adherence (PDF) guides researchers in a holistic review […]
Screening, Enrollment, and Master Log
Guide to Using the Screening & Enrollment Log (DOC) Screening & Enrollment Log Template (XLS)
Visit the LARS Project page.
FDA Audit Checklist
Download the FDA Audit Checklist: From Notification through Close-Out (DOC).
CIRC Disclosure Review Process
Created 01.15.2020 Introduction The WUSTL Research Conflicts of Interest Policy states “The Conflicts of Interest Review Committee(s) (CIRC) is the designated official(s) responsible for evaluating financial disclosures.” This procedure outlines the process that the CIRC uses to evaluate the disclosures for financial conflicts of interest (FCOI). Disclosure Review All covered individuals are required to submit […]
Protocol Templates for Clinical Trials (NIH Templates for both biomedical and behavioral & social sciences research involving human subjects)
See NIH protocol templates for both biomedical and behavioral & social sciences research involving human subjects.
Human Subjects Education and GCP Training Requirements Diagram
See the diagram on the differences between Human Subject Education and Good Clinical Practice training requirements in Box.