Our services include:

  • In-vitro and in-vivo bioequivalence studies
  • Clinical trials
  • Simulation/ Monte Carlo studies, Monte Carlo and randomization tests, bootstrap, outlier identification and analysis, QC/QA reporting requirements, DOE, stability analysis, microbiological environmental monitoring, analysis and reporting (air, water, machines), FMEA analysis, etc.
  • Tailored training in statistics
  • Consultation services geared to the client's level of expertize
  • Urgent turn-around times

Cair Center has accumulated vast experience in several therapeutic areas including respiratory diseases, allergy, asthma, oncology, gynecology ,etc..
Our primary tasks have been to participate in successful global regulatory submissions by taking responsibility for statistics, data management, and preparation of reports on a timely bases.
We have also on occasions participated in meetings with the EMA.

Currently, we are participating in several drug development projects aimed at regulatory submissions.