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invivodata and PRO Consulting to Present at International Industry Events
Date:3/2/2009

PITTSBURGH, March 2 /PRNewswire/ -- invivodata, inc., (http://www.invivodata.com) the industry leader in electronic patient reported outcomes (ePRO) solutions and services for global clinical research, today announced a series of featured presentations at upcoming international events to be delivered by representatives from invivodata and its scientific and regulatory consulting division, PRO Consulting(R) (http://www.patientreported.com).

Scientific, regulatory, and technical experts from invivodata and PRO Consulting will share their knowledge on the collection of Patient Reported Outcomes (PRO) data and e-clinical technologies at the following industry events:

  • Association of Clinical Data Management (ACDM) Annual Meeting (8-9 March 2009 in Northamptonshire, UK). invivodata's Adam Wood will present "ePRO Evolution and its impact on Clinical Data Management".

  • Drug Information Association (DIA) Annual EuroMeeting (23-25 March 2009 in Berlin, Germany). invivodata's Vice President, Europe and Asia Pacific, Dr. Wolfgang Summa will present "Integration of Direct Data Capture, ePRO and EDC Data via CDISC ODM".

  • Annual eClinical Trials Conference (13-14 May, 2009 in London, UK). Dr. Wolfgang Summa will present "The Impact of CDISC on e-Clinical Trials" at Vision in Business' conference.

  • International Society for Pharmacoeconomics and Outcomes Research (ISPOR) Annual International Meeting (16-20 May, 2009 in Orlando, FL). PRO Consulting Scientist, Dr. Chad Gwaltney will lead a workshop presentation on "Establishing the Content Validity of PRO Instruments".

Pharmaceutical research professionals can also learn more at ePROficiency(TM) 2009, invivodata's annual Patient Reported Outcomes Conference (http://www.invivodata.com/ePRO2009). Attendees of this conference, which begins April 21, 2009 in Naples, FL, can participate in general PRO sessions and various peer-led tracks focused on PRO regulatory guidelines and implications, industry and scientific trends, and best practices for designing and executing ePRO systems in clinical research.

Additional information on ePROficiency 2009 and other upcoming presentations by invivodata and PRO Consulting scientists can be found at http://www.invivodata.com/news-events/events or www.patientreported.com.

About invivodata, inc.

invivodata combines behavioral science, information technology, and clinical research expertise to capture high quality clinical trial data directly from patients. invivodata's electronic Patient Reported Outcomes (ePRO) solutions, which are based on over 20 years of research, deliver reliable patient self-reported data by driving patient compliance with the protocol and eliminating recall biases that plague paper-based self-report data. invivodata's solutions include comprehensive trial-support services that facilitate the collection of ePRO data, web-based access to study data and operational reports that give researchers and sponsors visibility into study progress, and scientific and regulatory consulting on the use of PRO data in a regulated environment. invivodata's solution has been used in more than 275 clinical programs and is the industry-leading ePRO system in delivering primary efficacy data for FDA drug approvals. invivodata inc. is a privately held company with global headquarters in Pittsburgh, Pa., USA; its European headquarters is in London, England; and its technology development center is in Scotts Valley, Calif., USA. For more information visit www.invivodata.com.

About PRO Consulting

PRO Consulting, a division of invivodata, inc., provides consulting services to help clinical research teams effectively develop, execute, and document patient reported outcome (PRO) strategies to support their clinical research objectives. The PRO Consulting team has more than 140 years of cumulative experience in psychometrics, PRO study design, migrating and validating electronic solutions to collect PRO data, and has extensive experience working with the FDA and other regulatory bodies. For more information please visit http://www.patientreported.com.

    For more information, contact:

    Invivodata, inc.
    Christine Tobin
    Corporate Communications Specialist
    (412) 390-3000, ext. 3502
    ctobin@invivodata.com


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