Initial IRB Submission: 7 Fundamentals Of Success

A successful initial Institutional Review Board (IRB) submission is crucial for launching a clinical trial without unnecessary delays. Ensuring approval on the first submission requires a strategic approach that prioritizes completeness, clarity, and responsiveness. This article outlines seven key fundamentals for optimizing IRB submissions. Find out how adhering to these principles allows researchers to streamline IRB approvals, keeping their clinical trials on track.

• Pre-screening support before submission
• Utilize easily understandable informed consent forms
• Avoid piecemeal submissions to minimize resubmissions
• Maintain Open communication with all stakeholders
• Maintain responsiveness and submission momentum
• Employ a user-friendly IRB submission system
• Support your submission process with flexible IRB