Protecting the rights of patients and patient safety is at the heart of any clinical trial. That’s why the Institutional Review Board (IRB) reviews and approves research studies before they begin to ensure that they meet ethical standards and minimize risk to participants and patients. It is a process essential to scientific research. It’s also a process that requires extensive documentation, so small submission mistakes, from omitted attachments to inconsistencies, can lead to delays. This infographic is a checklist for staying organized when submitting to an IRB to keep studies moving without compromising ethical rigor or regulatory compliance. A partner can help you move through that process with confidence and efficiency while avoiding common pitfalls. Highlights include: The key forms and other documentation that are critical for study teams, sponsors, and CROs. The required documentation that is specific to research sites. Identifying common IRB submission mistakes.
