Empower Your Biomedical Research & Clinical Trials

EMMES offers a complete information technology solution in support of all phases of medical research and clinical trials to pharmaceutical and biotechnology companies; academic and medical research institutions, non-profit organizations and government. Your project benefits from rapid clinical study definition, timely high quality data and efficient processes for improved productivity. The EMMES Corporation's ability to achieve these objectives stems from close to three decades of experience working with sponsors in the areas of protocol development, data collection and management,statistical analysis and regulatory support for clinical studies.

EMMES Advantage Suite, the umbrella information technology offering includes our web-based platform for data capture and management allows sponsors, protocol monitors, medical researchers and coordinators to quickly deploy projects, rapidly respond to changes in the protocol, and make intelligent decisions based on quality subject data.

Our flagship application,EMMES AdvantageEDC^SM, is an effective tool that helps sponsors safely conduct clinical studies while meeting the time and business commitments required to bring products to market. A comprehensive platform providing study design tools, timely data collection in sophisticated eCRF's,data quality management,a vast array of reporting options including critical outcomes like Adverse Events and online monitoring to improve overall execution of biomedical research projects.

With over 25 years experience, our track record is demonstrated by our successful implementations:

• Currently in use in over 40 clinical trials and medical studies
• Over 220 Protocols
• Over 1000 medical sites, laboratories and repositories worldwide

Each study has unique characteristics and correlations that need to be uncovered as the project progresses. The EMMES Integrity^SM the ideal quality control tool for specifying deficiency conditions enables the assessment of unusual data trends and patterns enabling you to quickly identify data anomalies.

EMMES GlobalTrace^SM, a premier materials management capability tracks specimens in real-time, from the time of collection at a clinical site to the arrival at a central laboratory or repository which is essential for many research projects and clinical trials. Deployment of GlobalTrace provides collaborating sites with a comprehensive specimen shipping and inventory system that will facilitate material handling from originating to other participating locations.

EMMES Advantage Suite provides a complete technical solution for your data collection and data management needs. The applications are hosted in EMMES secure data center. Of importance to your project is that your project data conforms to 21CFR Part 11 and other regulations.

Contact us today for a demonstration or so we can show you how EMMES Advantage Suite can meet your critical project objectives.

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