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About ClinicalTrials.gov

Instructions to register an RCMI-sponsored trial on ClinicalTrials.gov

 

The ClinicalTrials.gov Protocol Registration System (PRS) is a web-based tool developed for submitting clinical trials information to ClinicalTrials.gov. Records submitted through the PRS (http://register.clinicaltrials.gov) are available to the public at ClinicalTrials.gov. A guided tour of the PRS and account application information are available at http://prsinfo.clinicaltrials.gov/.

The Office for Research Compliance at the University of Puerto Rico sent a communication to ensure that applicable clinical trials are being kept in compliance with NIH standards and designating Ms. Gloria Cruz, UPR ClinicalTrials.gov Administrator. Ms. Cruz will provide assistance with account set up or password reset, registration of trials and results reporting of completed trials. Investigators must contact Ms. Cruz at to create a new account in the ClinicalTrials.gov Protocol Registration System (PRS). PRS users will then enter information about their clinical trials, ensuring that the information is correct, readily understood by members of the public, and updated in a timely manner.

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