The Copernicus Group IRB (CGIRB) Board is composed of a diverse group of men and women with the following backgrounds (view roster):

• Physician
• Ethicist/clergy
• Patient advocate
• Consumer advocate
• Attorney
• Scientist

Thoughtful ethical review provided by CGIRB is further enhanced by the support of knowledgeable professional staff members. What the client can expect is high quality work provided by one of the most comprehensive IRB services available in today's clinical research industry.

• Multiple CGIRB Board meetings each week (view schedule)
• 2-3 business day turnaround on documents
• Multi-center or single site reviews
• Online submission and tracking capabilities
• Continuing Review reminders sent to investigators
• The CGIRB Investigator Guidebook provided to each approved investigator (see forms)
• Education and training resources
• Certified Translation Services

• FDA and OHRP Regulated Studies
• Phase I-IV drug studies in all therapeutic areas
• Device Studies
• Biologic Studies
• Observational/Registry Studies
• Social-Behavioral Studies

Download a copy of our Brochure.

Download a copy of the CGIRB Compliance Statement.