Pearl IRB Policies
Welcome to working with Pearl IRB! Our goal is to provide you with the most efficient, quality review possible. One of the keys to success is clear communication and transparency. Click here to review our Submission Guide and Policies.
To assist our clients in meeting the reporting requirements for ClinicalTrials.gov we have developed a guideline to help you comply. Please review the guide here and don’t hesitate to contact us with any questions.
To view Pearl IRB’s Human Research Protection Program plan, click here. The purpose of this document is to describe our plan to comply with ethical and legal requirements for the conduct and oversight of Human Research.
For a complete list of our forms, click here.