Our Experience at the Service of your Clinical Data.

We will support you in every step during clinical drug development at the asset, indication, or protocol level

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Our Mission.

​Our Quantitative, Qualified & Quality-focused Scientists ​will provide solutions to help and  support Pharmaceutical companies, Biotechs,  MedTechs & CROs ​developing their product until regulatory approval & access to patient

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Our Experience.


Oncology, Immuno-oncology, Immunology, Metabolics, Cardiovascular and Neuroscience.

Study Phase

Phase II, III and IV.


Statistical expertise in numerous global regulatory submissions, (FDA, EMA, PMDA...), including Face to Face meetings.

HTA & Publications

Statistical support for submissions to several HTAs (AMNOG, HAS, NICE), reimbursement dossiers and scientific publications (NEJM, The Lancet, JCO ...)

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Our Services.

Biostatistics and Data Science Consultancy.


Statistical Support at the Asset level.

Statistical Support at the Protocol Level.   

Regulatory Interactions.

The 3 co-owners have over 60 years of combined experience in the Pharma industry.

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We bring our expertise in Quantitative Sciences to your drug development project.


Each team member comes with over 15 years of experience in the pharma industry.


We are committed to become trusted partner who designs and delivers high quality solutions.