A PRS individual (user) account is established when a principal investigator wishes to register one or more trials, without coordinating with other investigators within the organization. This allows entry of trial information to begin without delay. ClinicalTrials.gov then assists in identifying the appropriate individual(s) to act as PRS administrator for the investigator's organization.
In order to avoid duplicate registration and to ensure that the appropriate organization or investigator provides the information for each trial, please consider the following questions and take the suggested steps:
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