{"id":363776,"date":"2023-12-01T12:26:45","date_gmt":"2023-12-01T17:26:45","guid":{"rendered":"https:\/\/platohealth.ai\/fdas-estar-program\/"},"modified":"2023-12-01T15:22:31","modified_gmt":"2023-12-01T20:22:31","slug":"fdas-estar-program","status":"publish","type":"post","link":"https:\/\/platohealth.ai\/fdas-estar-program\/","title":{"rendered":"FDA’s eSTAR Program","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"

\"GMDP_346(1)\"<\/p>\n

This episode of the Global Medical Device Podcast delves into the world of FDA submissions, specifically focusing on the eSTAR program.\u00a0<\/p>\n

Host Etienne Nichols leads an insightful discussion exploring the intricacies, benefits, and strategies for using eSTAR effectively in medical device regulatory submissions.<\/p>\n

To discuss this topic, we brought in the following experts:<\/p>\n