The right approval, for the right use.

The IRB approval process can be one of the most time-consuming steps in launching a research project. In partnership with the Data Office for Clinical and Translational Research (DOCTR), our team consults with researchers ahead of submission to ensure protocols are well-prepared, clearly documented, and aligned with IRB requirements — reducing the back-and-forth that often delays approval. Whether you need guidance on study design, data use language, or documentation specific to AI and digital health research, we help you submit a stronger, more complete protocol the first time.