With clinicalRSVP’s fully-supported, Web-based system, your participant’s fingerprint is all it takes to securely and confidentially validate subject eligibility prior to enrollment. To improve safety, lower risk and defend the integrity of research in your studies, give dual enrollment the finger with clinicalRSVP.
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clinicalRSVP - Give Dual Enrollment the Finger | data-integrator.com Reviews
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With clinicalRSVP’s fully-supported, Web-based system, your participant’s fingerprint is all it takes to securely and confidentially validate subject eligibility prior to enrollment. To improve safety, lower risk and defend the integrity of research in your studies, give dual enrollment the finger with clinicalRSVP.
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clinicalRSVP Events and News
http://www.data-integrator.com/usNewsEvents.aspx
Read our last publication - "Research Participants Do Travel". August 09, 2012. ClinicalRSVP eNewsleter August 2012. August 09, 2012. ClinicalRSVP present at DIA 2012. June 25-27, 2012. ClinicalRSVP eNewsleter June 2012. June 22, 2012. Darran Boyer presenting at the ACPU Annual Meeting. April 25-26, 2012. Network of Innovator Sites Renew with clinicalRSVP’s Research Participant Registry. February 16, 2012. Visit us at Booth #135 at the ASCPT Annual Meeting. March 14-17, 2012.
About clinicalRSVP
http://www.data-integrator.com/usAbout.aspx
ClinicalRSVP was founded in 2008, in response to the needs of a group of investigators looking to prevent dual enrollment in their region of South Florida. Since then, clinicalRSVP has expanded across North America reaching as far north as Toronto, Canada, and as far west as San Diego, California. Today, clinicalRSVP operates the industry’s largest study participant clearinghouse in the US and Canada. Utilizing innovative, efficient, and confidential identification methods. Ft Lauderdale, FL 33301.
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Join the Race against Dual Enrollment.
clinicalRSVP - Give dual enrollment the finger
http://www.data-integrator.com/clinicalRSVPOverview.aspx
Clinical Research Subject Verification Program. ClinicalRSVP is a de-identified clearinghouse used by the clinical trials industry to authenticate that study volunteers do not participate in more than one clinical trial at a time. ClinicalRSVP utilizes a simple and secured approach that allows investigators to objectively authenticate study participant eligibility prior to enrollment by:. Utilizing biometric fingerprint technology. Maintaining a secured and blinded database validated according to 21 CFR.
clinicalRSVP - Give Dual Enrollment the Finger
http://www.data-integrator.com/Default.aspx
ClinicalRSVP stops dual enrollment by authenticating study participants in real-time with biometric fingerprint technology. Automated system maintenance and validation. Discrepancy resolution and 24/7 subject hotline. Secure, reliable data hosting. Usage reporting and monitoring. To access the clinicalRSVP database. FREE 90 DAYS TRIAL FOR SITES. ClinicalRSVP has zero start-up costs and no hidden fees. Read our last publication - "Research Participants Do Travel".
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clinicalRSVP - Give Dual Enrollment the Finger
ClinicalRSVP stops dual enrollment by authenticating study participants in real-time with biometric fingerprint technology. Automated system maintenance and validation. Discrepancy resolution and 24/7 subject hotline. Secure, reliable data hosting. Usage reporting and monitoring. To access the clinicalRSVP database. FREE 90 DAYS TRIAL FOR SITES. ClinicalRSVP has zero start-up costs and no hidden fees. Read our last publication - "Research Participants Do Travel".
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