This page contains information guides that can be useful when preparing a research protocol and informed consent for IRB review as well as implementing an approved research protocol. This page also contains information on the fees associated with sponsored clinical studies.

Informed Consent Guide

HIPPA Authorization Template and Revocation Template

Research Guides

Short-form Consent Template and Guide for Use with Non-English Speaking Research Subjects

Registering Investigator-Initiated Clinical Trials on

Guidelines for Investigators and Research Staff

Use of a  Central IRB

Contact Info

Theresa Greaves
LIMR Office of Research Affairs


Main Line Health