Postmarket Safety Surveillance of FDA-Cleared Prescription Digital Therapeutics Using the Manufacturer and User Facility Device Experience (MAUDE) Database: A Pharmacovigilance Study.
Major Depressive Disorder Literature
Publication date: Jun 01, 2025 Background and aim Prescription digital therapeutics (PDTs) are software-based medical treatments authorized by the U. S. Food and Drug Administration (FDA) for a range of ... Read more