Our Services

  • Clinical trial design –
  • Drug development plans from Phase I to Phase IV
  • Input to regulatory dossiers
  • Statistical representative for client at EMA, MHRA and FDA meetings
  • Assessment of probability of success for the next phase of development and criteria for continuation
  • Input to product profile and marketing material
  • Protocol development and review
  • Sample size calculations
  • Statistical analysis plan preparation
  • Statistical reports
  • CRF advice and review
  • Independent statistician for the DMC
  • Performing statistical analysis and statistical modelling
  • Statistical QC
  • Review of tables, figures and listings
  • Evaluation of in-licensing and due diligence
  • Statistical representative at advisory boards

Get In Touch.

If you are interested in working together, send us an inquiry and we will get back to you as soon as we can.

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