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eSimplicity Enterprise Clinical Research Solution by Medepresence is a single, integrated solution – offering a compelling suite of benefits traditionally requiring multiple solutions. eSimplicity conveys the benefits of Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and Clinical Data Management Systems (CDMS)

eSimplicity can significantly streamline the entire process, from patient enrollment to scheduling, patient data collection, investigator reporting, proactive monitoring & management.

This will result in better quality data collected at a lower cost to the Sponsor, with smoother study oversight and more efficient monitoring. We strive to advance the state of clinical research management –A Value Delivery Platform offering compelling clinical, financial and risk management benefits (more)

 
 Patient Enrollement
 Scheduling
 Data Capture
 Clinical Data Management
 Adverse Events
 Alerts
 Finance Module

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Patient Recruitment is critical to a successfull clinical study. Our flexible and highly configurable system supports Randomization (Control and Study groups), Inclusion-Exclusion criteria checks for eligibility, and a variety of other functions. Physicians can review patient data and approve patients for includion in study online - anytime and from anywhere.

Our powerful Scheduling system auto-schedules patients for collection of patient data based on surgery dates and at intervals as per study requirements. Again, study intervals are configurable so sponsors / CROs can configure study intervals as required.

Our unique and innovative Clinical Data Capture system called the Patient Wizard facilitates accurate data capture directly from the source - patients. Responses to SF36 and Oswestry forms are scored automatically and are ready for research analysts to perform further analysis and generate a variety of reports. Electronic CRFs allow online capture of clinical data required for the study.

Advanced tools facilitate effective data management. Data Collection screen displays different statuses of data collection for Investigators to review pending data collections and take necessary action to ensure timely data collection. The Navigation screen provides a summary view of a patient's data collection status across multiple encounters with quick links to a variety of CRF forms. The Analysis tool is yet another powerful tool to support analysis of data across multiple facilities and different study groups.

The highly configurable Adverse Event tool facilitates accurate capture and timely reporting of adverse events so Physicians and Sponsors may take timely and informed decisions. The system supports generation of adverse events reports satisfying regulatory requirements.

Our advanced Alerts tool generates a variety of alerts relating to scheduling and collection of patient data, adverse events and physicians/investigators are notified for timely action.

The Finance Screen gives a summary view of all Investigator payments across multiple sites so sponsors can review, track and ensure timely payments are made to Investigators.