Resources and Tools - CTD

um rcqa resources and tools

Researchers often ask what tools or resources are available to help navigate compliance with Clinical Trial Disclosure Requirements.  This page has been created so that research teams will have handy resources and tools available for use.  Additional resources and tools will be added continuously, so please bookmark the page!

An online survey that facilitates the determination if your study meets the requirements for registration on ClinicalTrials.gov per UM Policy HSR-P-101.

A link to the description and/or schedule for all of the classes offered for Clinical Trial Disclosure.

A visual aid to facilitate the completion of the ClinicalTrials.gov. PRS Oversight section.

A visual aid to facilitate the completion of the ClinicalTrials.gov. PRS Eligibility section.

A visual aid to facilitate the completion of the ClinicalTrials.gov. PRS Study Design section.

A checklist to facilitate the completion of the ClinicalTrials.gov. Results Reporting section.



A guided checklist of required elements to be included in a study record for protocol registration on ClinicalTrials.gov