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ePRO on Netbooks (NetPRO) - The BEST ePRO Solution for Clinical Trials in 15 Years
Date:1/12/2010

assisTek, the Leader in Innovative Electronic Patient Reported Outcomes (ePRO) Solutions and Patient Questionnaires for Clinical Trials announces NetPRO – ePRO on netbooks!

Scottsdale, AZ (PRWEB) January 12, 2010 -- assisTek announces its newest innovation in ePRO solutions today, ePRO on netbooks (NetPRO). With NetPRO, assisTek once again leads the ePRO and clinical trials market with solutions that bring SIGNIFICANT advantages to study sponsors and patients enrolled in clinical trials. NetPRO combines the advantages of the large screen of a touch screen tablet, the data communications of a cell phone, and the low cost of a PDA.

The Netbook (NetPRO) ePRO Solution offers many benefits to clinical trial sponsors. First, the netbook offers the sponsor unequaled access to data. With assisTek’s new NetPRO offering, all data gets transferred automatically through the local cell phone network. Clinical trial teams have vastly improved access to data compared to PDAs or Palm devices because there is no longer a delay between when patients enter data and when they actually transfer data (and they have remembered and have overcome their data transfer problems). 100% of data entered by patients is available to the study team at all times. This real time data access to 100% of the study data enables the study team to truly monitor compliance, assess study status, and manage the study real time.

Second, the netbook offers study sponsors outstanding data quality. Large screens with large font and buttons that are clearer and easier to use result in more accurate patient answers and higher quality data. Further, large screens enable all the relevant data on a single PRO concept to be captured accurately on a single screen. For example, the detail on a body pain diagram, a sleep scale, or a stool scale can be most easily seen on a larger screen, which enables the patient
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ePRO on Netbooks (NetPRO) - The BEST ePRO Solution for Clinical Trials in 15 Years
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