About Us

“Partnering with MedAware Systems allowed us to fastidiously and efficiently take an objective, methodological approach to a medical issue that has been vexing clinicians for over two decades. Nearly 1,000 publications were uncovered … allowing us to extract and synthesize data from these publications in the form of a meta (mega!) analysis – much faster than we would have been able to do ourselves…what might have traditionally taken years was completed in months.”
                                                                                         Seema Kumbhat, MD, Senior Vice President, Regional Medical Director, Fresenius Kabi

MedAware Systems, Inc. is a next generation medical research data company that empowers Pharma and Medical Device companies with all available evidence from published clinical trials research, event reporting databases (US, EU, Canada, Australia, Singapore, and others, worldwide), and social media.

The SOHInfo data and analysis platform delivers massive datasets in the shortest time frame in the industry. Data are meticulously extracted, organized, and standardized, and instantly available for reporting and analysis. The Company continuously updates data to provide you with the industry-standard  information resource.

Post Market Surveillance  SOHInfo Post Market Surveillance          SOHInfo Post Market Surveillance

For Researchers, Pharma and Medical Device Companies

With its patent-pending technology, the Company is currently addressing critical needs for Pharma and Medical Device companies. Current customers include: Abbott, Medtronic, Fresenius Kabi, Nestlé Health Science, Terumo Medical, Terumo BCT, Stryker Medical, and others. The Company uniquely addresses significant problems experienced by its customers, including:

  • collection and analysis of all published research data for regulatory filings
  • comprehensive and granular competitive analysis
  • evidence-based marketing messaging in highly competitive markets
  • due diligence for product or company acquisition
  • informing product development with analysis of all relevant published research

A Tremendous Resource for the EUMDR

The new medical device regulation in the EU (EUMDR), requiring re-certification of medical devices, comes with a hard deadline that is fast approaching. A key component of the EUMDR is its mandate for significantly more clinical evidence, especially for higher risk devices. Contact us for more information on how SOHInfo will provide significant value, in both time and cost, for your MDR filings.

Why MedAware Systems?

No competitor offers the speed, granularity, accuracy, and completeness of data, reporting, and analysis as MedAware Systems.

Utilizing our patent-pending software tools, processes, data analytics, and experienced staff we:

  • search and categorize the vast body of published clinical trials related to your specific products
  • ingest massive amounts of data from those trials in a remarkably accelerated time frame
  • and provide the most complete and granular analysis possible today

With comprehensive reports and analysis from MedAware Systems’ SOHInfo, you obtain greater insight into the efficacy and safety of your products than is currently available elsewhere. You are also able to identify reliable trends in patient outcomes as well as process additional data to uncover trends for specific cohorts and application settings.

Click here to learn about SOHInfo Literature Search and Analysis