CDRH promotes digital transformation.

The U.S. Food & Drug Administration’s (FDA) Center for Device & Radiological Health (CDRH) improved support for the medical device review process through an enterprise modernization initiative. The CDRH Progress Tracker (PT) portal provides a centralized, plain language, self-service touchpoint for medical device review processes – using a low code platform capability to accelerate application development and increase user productivity. Join this session to see how PT re-envisioned how CDRH interacts with medical device manufacturers worldwide, using a secure cloud-based solution and significantly improving the customer experience.