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Why Go with BeyondEDCTM eClinical Suite (Mi-Forms)?

Browser-based EDC systems still mean paper worksheets for sites, with data manually entered days or weeks after collection. Eliminate manual data entry processes with BeyondEDCTM Mi-Forms "point of contact" data collection, seamlessly integrated to your EDC or CDMS system. Reduce study cost and improve availability of data. eClinical data collection for Tablet PC and Digital Pen. Learn more about our solutions.


"Mi-Forms' open, standards-based architecture allows it to easily integrate with our EDC system, and eliminates the pains and costs associated with paper-based source documentation and paper CRFs for our end users."
EDC Company Founder

"The sponsors have certainly increased the data entry burdens on us by requiring EDC. Our study coordinators are over-whelmed - in one study we saw a 51 day delay between the patient visit and the EDC data entry. Mi-Forms makes our lives easier by allowing point of contact collection of research data in immediate electronic format."
Site Owner

Are you having data-entry challenges with your EDC system? Read Mi-Co’s free white paper, "Resolving Data-Entry Challenges Faced by EDC Systems in Clinical Trials" here. Click here



Welcome to the www.beyondedc.com website, where you will find pen-based electronic data collection solutions to your clinical trial data collection challenges. Mi-Forms data collection software and solutions automate paper collection processes via user-friendly handwritten electronic forms, reducing errors and costs and speeding up availability of data for review. Mi-Forms pen-based data collection solutions offer an easy, natural system for collecting electronic data immediately at the point of data generation, on-line or off-line. Mi-Forms for Tablet PC and Digital Pen provide powerful advantages over ordinary paper, traditional double-key and web-based data entry in eClinical applications such as Site Visit Reporting, Electronic Case Report Forms (eCRFs), Informed Consent Forms (ICFs), and Electronic Patient Reported Outcomes (ePRO). In addition, Mi-Forms solutions have been used to automate paper processes in pharmaceutical manufacturing quality assurance.

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Mi-Co Attends the Association of Clinical Research Professionals 2010 Meeting in Tampa, FL

Mi-Co & FedResults Host Breakfast Briefing “Computing on the Go: The Evolution of the iPad, Tablet PCs and Digital Pens”

Mi-Co’s Mi-Forms Validated for FDA Regulation 21 CFR Part 11 Compliance

Mi-Co is a member of the Medidata Developer Central, an online developer community dedicated to users of the Rave Web Services API. The Medidata Rave Web Services API allows external systems such as Mi-Forms to be seamlessly integrated with market-leading Medidata Rave®, including inbound and outbound data sharing using CDISC* data standards. Please see http://www.mdsol.com/innovate/index.htm for more information.


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