{"type":"video","version":"1.0","html":"<iframe src=\"https://www.loom.com/embed/02376bbed49147099608a5a8c941e28e\" frameborder=\"0\" width=\"1920\" height=\"1440\" webkitallowfullscreen mozallowfullscreen allowfullscreen></iframe>","height":1440,"width":1920,"provider_name":"Loom","provider_url":"https://www.loom.com","thumbnail_height":1440,"thumbnail_width":1920,"thumbnail_url":"https://cdn.loom.com/sessions/thumbnails/02376bbed49147099608a5a8c941e28e-00001.gif","duration":294.424,"title":"How to Use Atlas to De-Risk Regulatory Acceptance","description":"In this video, I will discuss how to use Atlas to de-risk regulatory acceptance. The primary driver for your team is to derail the likelihood of regulatory approval once submitted. Staying up to date with current information is a challenge in the regulatory process, but Atlas provides the most comprehensive network of evidence across therapeutic areas and medical conditions. Precision measurement trials are complex, and implementing DHTs can improve recruitment, retention, and generalizability of data. With the volume of literature generated each year, it's difficult to stay up to date, but Atlas saves time by providing access to the right data and standardized ontologies."}