Technical Resources International, Inc. (TRI)

Technical Resources International, Inc. (TRI)

As an award-winning, minority-woman-owned contract research organization (CRO+), TRI supports clinical research in the United States and around the world, by providing clinical research, information technology, and communications services.

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Locations

  • Africa
  • Asia including Japan
  • Europe
  • North America
  • South America

Therapeutic Areas

  • Cardiovascular
  • Infectious Diseases
  • Medical Device
  • Obstetrics / Gynecology
  • Oncology
  • Orphan Drugs
  • Pediatrics / Neonatology
  • Substance Abuse
  • Vaccines

As an award-winning, minority-woman-owned contract research organization (CRO+), TRI supports clinical research in the United States and around the world, by providing clinical research, information technology, and communications services. For 44+ years, TRI has served government agencies, private industry, and non-profit organizations. TRI is headquartered in Bethesda, Maryland with multiple global offices. TRI’s clinical research solutions support observational and interventional clinical trials, Phase 1– 4, covering a variety of therapeutic areas and drug, biologic, and device products. Our technology solutions create matchless user experiences through responsive design and optimized web development. TRI’s certified, secure Agile practices deliver better value faster maintaining compliance in a regulated industry. Our communications solutions deliver and analyze participant recruitment and multilevel event planning services with engaging designs by implementing full-service marketing and outreach across all media.

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 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 targeted source document verification (TSDV) application, process optimization, and scope of TSDV services. This Accreditation teaches Partners to implement TSDV in line with regulatory compliance and data quality strategies. TSDV Accreditation is dependent on the successful completion of the Rave EDC Accreditation.