Yossi Tal has been working with the life science industry for over 15 years. He has a BSc from California State University and a Doctorate from Northwestern University, Illinois, USA and was a statistician at the US National Institutes of Health, before forming his own company, based in Israel, providing bio-statistical services for regulatory submissions for both devices and pharmaceuticals.

Dr Tal’s services cover all statistical aspects of clinical studies, including: pre-clinical and clinical study design, protocol statistical analyses, ongoing statistical consulting, data management (Clinplus software, 21 CFR 11 compliant), statistical analysis plans and analyses, regulatory reporting and representation, advisory and data monitoring committees, and bio-statistical training.

He lectures extensively on statistics for non-statisticians and wrote ‘Reading Between the Numbers: Statistical Thinking in Everyday Life’ (McGraw-Hill, 2001), in addition to authoring over 50 articles on statistics.

Dr Tal can help you with:

  • Development of statistical analysis plans
  • Statistical analysis of results
  • Authoring of the statistical section of final study reports, including relevant explanatory tables and results listings
  • Development of a data management plan
  • Set up of data structures
  • Full data management service