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ArticleCureus2025

Postmarket Safety Surveillance of FDA-Cleared Prescription Digital Therapeutics Using the Manufacturer and User Facility Device Experience (MAUDE) Database: A Pharmacovigilance Study.

Shaheen E LakhanPubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 40469887