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Our Approach

our approach

Brightech is trusted by big pharma not only for our statistical expertise, but also because of our proactive, partner-like approach with each of our clients.

This approach is driven by the combination of our unique people, processes and systems that have been validated by the FDA and EMA in over 400 clinical studies.

People

  • Over 130 employees in the U.S., China and Taiwan
  • Capable for global studies in multiple languages including English, Chinese, Japanese, and Korea
  • 24/7 round-the-clock services
  • Scalable as needed
  • Our 10 PhD statisticians and Innovative Trial Design Group overseen by KOLs positions Brightech as the only company that knows the FDA regulation, the proper statistical approach

Processes

  • Optimized timeline from start-up to database lock
  • QC documentation
  • Flat management structure; no “big” CRO multi-layer setups

Systems

  • CIMS (a proprietary integrated system comprehensive and fully customizable web-based clinical trial platform)
  • SAS-based Statistical Reporting System, which efficiently generates submission-quality tables, figures, and data listings
  • Inform and Rave
Since 2002, Brightech has served 100+ clients and has completed 400+ projects in all phases. This gives our partners the assurance that my study is in good hands that we can always rely on Brightech.