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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!
clinicalRSVP ensures that volunteers only participate in one clinical trial at a time, protecting their health and maintaining data integrity for accurate research outcomes.
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.
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.
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.
No, clinicalRSVP doesn’t store participant names or collect study data. All relevant study data stays with the research site managing the clinical trial.
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