Clinical-grade patient data with built-in blinding for research integrity.
Prima for Research Patients
Research patients in Prima can carry the full complement of clinical patient information, but Prima supports study blinding through the use of a study-specific identifier. When a study is blinded, subject identity is replaced by the identifier across the interface and reports, protecting the integrity of the research while keeping data complete and fully traceable. Unblinding is managed through appropriate access controls. Research patients can also be linked to external systems via EMR numbers and alternate identifiers, making Prima a natural fit alongside existing clinical infrastructure.
Fields Prima tracks
Research Patients data captured and searchable throughout the workflow.
Patient Identifier (for fully blind)
Alternate Identifier
Name
Gender
Date of Birth
MRN / EMR Number
Study
Cohort / Group
Diagnoses