AI-Powered Insights, Unmatched Performance


Maximize Value From Data

Clinical Trials
MedAware Systems’ Science of Health Informatics (SOHInfo)™ delivers detailed data, information and analysis from published literature, reported regulatory events and social media. AI-based data & analytics provide comprehensive support for regulatory submissions, post market surveillance, scientific publications, R&D, and other business requirements.  Learn More…


Optimize Your Business Intelligence

                                                                     FAERS MAUDE
dvanced Surveillance of Clinical Trials Research, Event Reporting Databases – such as FAERS and MAUDE –  and Social Media for: Post Market Surveillance, Regulatory Filings (CERs, 505(b)(2), and 510Ks, EUMDR, ICSRs, ASUP, PMCF etc.); competitive analysis and marketing messaging;  due diligence; and informing new product development with all available published research and Regulatory AE reporting.  Learn More…

Real World Evidence

Clinical Trials data
MedAware Systems boasts the most experienced team in medical research data aggregation and analysis in the world. This capability provides you with all available Clinical Trials Evidence (CTE) data and, now, Real World data from Regulatory Databases and Social Media – What could you do with all of the data?

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