Electronic Informed Consent for Clinical Trials: Why, What and How - Webinar by GlobalCompliancePanel
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Website http://bit.ly/1843Xc4 |
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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 participationNeed for greater patient involvement during trialNeed to explain complex terms and protocolNeed to implement remote monitoringWhat concerns you the most: Reaction of the IRBFDA non-acceptance of the consentsPatient inability to use technologyLack of acceptance by clinical staffCostTimelinesAreas Covered in the SessionUsing an e-consent to assist low literacy patient populations understand your trialUsing e-consent to assist patients in understanding their role in a complex clinical trial.Working with an IRB in the review of a e-consentUnderstanding the cost drivers of an e-consent processFeatures of an e-consent. Deciding what is important to your trial.Who Will Benefit:Clinical trial Innovation teamsVP, Clinical trialsClinical Operations (VP, Senior Managers, Trial Managers)IT innovation leadsManagers, VPs Research PortfoliosDr. 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:800-447-9407Fax: 302-288-6884webinars
globalcompliancepanel.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.
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