Subject Safety and Study Data Integrity in clinical trials becomes compromised when research subjects participate in multiple overlapping clinical trials simultaneously.
clinicalRSVP tracks key enrollment dates and washout periods of research subjects across all phases of clinical trials while collecting zero study data to securely ensure the subjects don’t dual enroll in overlapping studies or re-enroll in the same study twice.
clinicalRSVP raises the bar for study data integrity and participant safety
The following best in class features allow Sites to focus on recruitment and enrollment and leave the rest to us.
The Industry is
Taking Notice
"clinicalRSVP elevates industry standards for authenticity and confidentiality, empowering researchers to confidently navigate the complex enrollment practices in clinical trials without compromising the integrity of the trails."
Patented Technology
since 2009
clinicalRSVP is the original dual enrollment prevention service provider and the first to receive a patent for the technology (2009). If you use dual enrollment prevention methods provided by other vendors that are similar to those described by clinicalRSVP and are concerned you may be in violation of the patents listed above, please contact us for additional information.
Lungescu et al., US. Patent No. 10,783,598 https://patents.google.com/patent/US10783598B2
Lungescus et al., U.S. 11,556,893 https://patents.google.com/patent/US11556893B2
Lungescu et al., US 12,159,261 https://patents.google.com/patent/US12159261B2
Questions?
Get in touch with our team
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We engage at all levels – Sponsors, CRO‘s, and Sites.
Bulster your commitment to data integrity and research participants safety today.
Have any questions?
If you’re volunteering for a clinical trial using clinicalRSVP, it’s important to understand how the platform protects your rights, privacy, and safety, along with the public’s well-being. Below are key FAQs to keep you informed.
Thank you for your contribution and help to advance research!
What is the purpose of clinicalRSVP?
clinicalRSVP ensures that volunteers only participate in one clinical trial at a time, protecting their health and maintaining data integrity for accurate research outcomes.
Why is study data important, and how does clinicalRSVP help?
The FDA requires reliable data to approve new drugs. clinicalRSVP ensures participants don’t join multiple studies simultaneously, preventing data inaccuracies and maintaining study compliance.
How does clinicalRSVP improve participant safety?
It ensures volunteers meet eligibility criteria and reduces risks by checking participation across studies. Volunteers should still review study risks with research staff before joining.
What is the purpose of the fingerprint scan?
Fingerprint scans confirm participant identity without storing biometric images. Only a unique code generated from the fingerprint is saved to maintain private and accurate identification.
Does clinicalRSVP store participant names or study data?
No, clinicalRSVP doesn’t store participant names or collect study data. All relevant study data stays with the research site managing the clinical trial.