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
Part 11
Authorizing access to data according to the needs and rights of stakeholders
Deploying expert administrator capabilities and clinical support
The goal of clinicalRSVP is to improve the clinical trials landscape for all stakeholders by preventing dual enrollment. The prevention of dual enrollment leads to increased accuracy of clinical trial study data and improvement of participant safety.