Way To Health specific documents & templates for IRB submission
All research studies need to submit documentation around the appropriate policies and procedures implemented to protect the rights and welfare of humans participating as subjects in the research. To accomplish this, IRBs use a group process to review research protocols and related materials (e.g., informed consent documents and investigator brochures) to ensure protection of the rights and welfare of human subjects of research. For research studies using the Way To Health platform, we have prepared a set of documents and templates to accompany the submission.
Variants of these documents have been reviewed and approved by the University of Pennsylvania's Institutional Review Board.Click the title to download
This document outlines how Protected Health Information is stored, secured and accessed on the Way to Health platform.
This is a template document provides a sample IRB protocol for a study using Way to Health. It includes details such as study design, recruitment strategies and examples of informed consent.
This is a template document that provides a framework for wording and content that the participant facing content. Please update with specific study content as appropriate.