Services Overview

At Technical Resources International, Inc. (TRI), true competitive edge resides within our Clinical Research, Communications, and Information Technology services staff. Our technical and communications skills are defined by experienced technical and medical writers, clinical research specialists, RNs, certified clinical research associates, regulatory compliance specialists, editors, information and database managers, event planners, video producers, and graphic designers, all working as one to realize your business objectives. TRI's complementary approach to problem-solving, powered by the unified strength of its three operating divisions, ensures your organization's success every time.

Key Services

  • Clinical Research Services
    • Clinical Operations
    • Data Management and Biostatistics
    • Regulatory Affairs and Medical Writing
    • Safety and Pharmacovigilance
    • Toxicovigilance and Health Assessment
    • Quality Assurance
  • Product Development
    • Phase I-IIs
    • Phase II-III
    • Phase IV
  • Communications
    • Market Research
    • Strategic Planning
    • Advertising and Public Releations
    • Scientific and Medical Events
    • Training
    • Multimedia Design and Production
  • Information Technology
    • Systems Integration
    • Business Intelligence for Clinical Research
    • Custom Applications Development
    • Validation of Regulated Clinical Systems
    • Clinical Systems Best Practices Consulting

Based on our international work, TRI’s project teams are especially knowledgeable about developing countries’ regulations and cultural differences, and have developed effective remote (also called central) monitoring procedures and tools. At any given time, TRI CRAs monitor more than 75 studies and review more than 1500 regulatory documents per month. To meet our clients’ needs, we provide our clinical operations services individually or as part of a package.

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