RSVP
RSVP (Research Subject Verification Program) is a web based central database used to track the dosing dates of Phase 1 research subjects to prevent them from participating in multiple research trials simultaneously and from by-passing required protocol wash-out periods. Recently, Clinical Pharmacology of Miami, along with other Phase 1 research sites in South Florida, agreed to report the dose taken date(s) of subjects participating in Phase 1 drug studies to RSVP. By reporting these dates, sites on RSVP can access the subject registry at the time of screening to help determine the last time a potential participant received dosing of investigational medication.  The subjects are identified by digitizing their fingerprint which generates a unique 9 digit number.  The result of implementing RSVP, is that cleaner subject populations are selected for studies. Sponsors that contract sites using RSVP know their data comes by way of subjects that undergo thorough screening measures to eliminate participation in more than one study simultaneously or before an appropriate washout.

For more information, please follow the link below:
WWW.CLINICALRSVP.COM