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Device Adverse Event Predictor

App

Predicts potential MAUDE-reported risks for new medtech prototypes using historical device data.

database 2 Dataset(s) Used

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Datasets

FDA CFR Title 21 Volume 8 business FDA ClinicalTrials.gov Registry business NIH/NLM FDA Drugs@FDA Database business FDA FDA Adverse Event Reporting System (FAERS) business FDA FDA MAUDE Database (Medical Device Reports) business FDA FDA National Drug Code (NDC) Directory business FDA PubMed Biomedical Literature business NIH/NLM MEDLINE Biomedical Bibliographic Database business NIH/NLM CMS Medicare Part B Drug Spending business CMS CMS Medicare Part D Prescription Drugs business CMS CMS Medicare Provider Utilization business CMS WHO Global Health Observatory business WHO WHO ICD-11 Classification business WHO WHO ATC/DDD Drug Classification business WHO WHO Immunization Data business WHO WHO Mortality Database business WHO

Apps

Clinical Trial Analyzer Dataset Explorer Product Similarity By Patent Launch Requirements Planner Clinical Trial Support/Opposition MedDevice Reg Compliance Checker Device Adverse Event Predictor Device Trial Designer MedTech IP Overlap Scanner Device Market Reimbursement Mapper MedDevice Provider Adoption Analyzer Device Safety Benchmark Tool MedTech Global Launch Planner Device Innovation Literature Scout MedTech Funding Risk Assessor

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