Biorasi

Biorasi is an award-winning Clinical Research Optimized™ CRO, offering project management, monitoring, safety, regulatory and data management services for its partners in the clinical research industry. From phase I-IV design to execution success, both single-study and program-wide optimization is obtained through ProAct+™, the most robust and innovative operating platform available. Equipped with ProAct+, Biorasi's full service project teams have developed numerous drug, biologic and device programs for FDA, EMA and other global regulatory agencies. Biorasi is headquartered in Miami, FL and has regional offices and operations across North America and around the world.

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Locations

  • Africa
  • APAC
  • Australia
  • Europe
  • North America
  • South America

Therapeutic Areas

  • Dermatology
  • Immunology
  • Nephrology
  • Neurology
  • Oncology
  • Woman's Health

Accreditations

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.
Partners are trained on the functionality of the eCOA application, best practices, process optimization and the scope of eCOA services. This Accreditation teaches Partners to process patient data that has been entered by the patient themselves, or by a Clinician. Patients enter their patient data through a provisioned device or their own device after downloading the appropriate app.  Clinicians enter patient data through a provisioned device (Android or iOS). eCOA Accreditation is dependent on the successful completion of the Rave EDC Accreditation.
Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.
Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.