Durham, NC. (February 10, 2010). eCliniqua, a leading online publication for clinical research by Bio-IT World, published a commentary today by Mi-Co titled “Pen-based site visit reporting solutions”. This commentary addresses the growing need for efficiency for a Clinical Research Organization (CRO)’s clinical monitoring processes to be streamlined, in order to turnaround trip report data quicker and reduce billing cycles. According to author Gautham Pandiyan, “In an industry where completing a trial a month early could mean millions of dollars of additional revenue for a sponsor, and the competition amongst CROs is intense, unique technology solutions such as Mi-Co’s eClinical Site-Monitoring solutions can give CROs the edge to leapfrog their competitors.”
The commentary can be accessed online at eCliniqua at the following URL:
To learn more about eClinical Site Monitoring solutions please contact a team member at firstname.lastname@example.org. More information about Mi-Co’s eClinical offerings can be found at www.beyondedc.com.
Mi-Co, a leading provider of mobile data collection solutions, provides software to automate paper forms-based business processes. Mi-Co’s enterprise Mi-Forms Software System provides flexible electronic forms design for data capture using digital ink and has proven capabilities for handwriting interpretation and verification, data validation and the communication of forms-based data. Mi-Forms support Tablet PCs, Digital Pens, Pocket PCs, signature capture devices and industry standard software technologies. Mi-Co is an Anoto Certified Partner delivering Digital Pen solutions since 2003. Mi-Co’s Mi-Forms is FDA 21 CFR Part 11 and HIPAA compliant and reaches historically paperwork intensive markets within healthcare including clinical trials, hospitals, pharmaceutical companies and more. The company is headquartered in Durham, North Carolina with a customer service center in Seattle, Washington. For more information on Mi-Co, visit www.mi-corporation.com
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eCliniqua provides authoritative news, views, insights and opinion on challenges related to clinical research, clinical trial design, data management and technology solutions. Written by a superb tandem of expert clinical reporters, eCliniqua highlights innovations in development planning and protocol design; new approaches to sponsor-CRO and sponsor-site relationships; novel patient recruitment and retention strategies and practices; project management; emerging and established electronic clinical trial technologies and standards; regulatory trends and compliance; pharmacovigilance; and much more.