Pearl IRB’s staff of experts offers a wide array of consulting, education, and staffing services for investigators, local IRBs, and sponsors. Pearl IRB can help you write your protocol and your consent form, provide regulatory support, and help you staff your study site.
Our staff has decades of IRB and research experience and their expertise ranges across therapeutic categories, drugs, biologics, devices, and all phases of research. We serve large and small institutions, principal investigators, CROs, and sponsors.
Core service offerings include:
Pearl IRB believes that complete and accurate preparation of study documents is key to getting a study initiated in a timely manner. We are willing to work with you up front to ensure that submission materials are ready for a successful IRB review.