Biotrial Biometrics Unit is part of the Biotrial Group and provides a fully integrated support / services for Non-Clinical to Phase I-IV trials for global sponsors

Our highly-skilled team of over 50 professionals the Biometrics Unit has more than 25 years of experience in both in-house clinical trials as well as large multinational trials.

With over 130 projects handled each year, our Biometrics Unit activity is in constant growth. It benefits from the close and constant relations with our medical and scientific experts.

We offer a full range of integrated solutions

  • Non-Clinical Studies
  • Phase I – Full-Package / stand alone
  • Phase II / III / IIIb Trials
  • Epidemiological Surveys, Post-Marketing Surveillance
  • Observational Studies


Our range of services includes:

  • Clinical Data Management
  • Coding
  • Biostatistics
  • Pharmacokinetics
  • Medical Writing



Our team consists of experienced, dedicated and highly-skilled team of Data Managers, Biostatisticians, Pharmacokineticists, and Medical Writers.


Biotrial Standards


  • Medidata RAVE
  • CDISC compliant (SDTM, ADaM, SEND)
  • Open CDISC tool to verify CDISC compliance
  • ICH E9
  • FDA 21 CFR Part 11

Our Biometrics Team can help you at any stage of your project and respond with a personalized work adapted to your needs.

For more information on our Biometrics Unit please contact us: contact@biotrial.com