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    Electronic Informed Consent for Clinical Trials: Why, What and How - Webinar by GlobalCompliancePanel

    View: 209

    Website http://bit.ly/1843Xc4 | Want to Edit it Edit Freely

    Category Webinar, Health, Medical, Pharma, Clinical

    Deadline: December 09, 2013 | Date: December 09, 2013

    Venue/Country: Fremont, CA, U.S.A

    Updated: 2013-11-13 15:41:59 (GMT+9)

    Call For Papers - CFP

    Overview: This webinar will present an exploration of trends that are leading to adoption of e-consent; options are available for e-consent, what is involved in implementing e-consent. A live demonstration of an e-consent will set the stage for implementation questions.

    Why Should You Attend : Why are you considering e-consent:

    Lack of patient interest in trial participation

    Need for greater patient involvement during trial

    Need to explain complex terms and protocol

    Need to implement remote monitoring

    What concerns you the most:

    Reaction of the IRB

    FDA non-acceptance of the consents

    Patient inability to use technology

    Lack of acceptance by clinical staff

    Cost

    Timelines

    Areas Covered in the Session

    Using an e-consent to assist low literacy patient populations understand your trial

    Using e-consent to assist patients in understanding their role in a complex clinical trial.

    Working with an IRB in the review of a e-consent

    Understanding the cost drivers of an e-consent process

    Features of an e-consent. Deciding what is important to your trial.

    Who Will Benefit:

    Clinical trial Innovation teams

    VP, Clinical trials

    Clinical Operations (VP, Senior Managers, Trial Managers)

    IT innovation leads

    Managers, VPs Research Portfolios

    Dr. Brink co-founded ConsentSolutions, Inc. in 2006 to further the development of media-based approaches to informed consent for clinical trials. She is the CEO and President. The company grew out of Phase II SBIR NCI funding for the development of an online informed consent process for clinical trials, on which she was the PI. Dr. Brink has authored articles in peer-reviewed publications discussing the effect of media on the patient experience, the need for e-consent, and the pathways to implementation of electronic informed consent in clinical trials.

    NetZealous LLC,

    DBA GlobalCompliancePanel

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA

    USA Phone:800-447-9407

    Fax: 302-288-6884

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/1843Xc4


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.