About us

Our strong expertise to support your clinical development projects

We support your clinical projects with our expertise in biostatistics, statistical programming, CDISC and consulting services

We offer our broad experience at various stages of clinical development, from Phase I to Phase IV trials, ISE/ISS, DSUR, PSUR, registries and across many therapeutic areas (e.g. neurology, rare diseases, oncology, respiratory diseses, dermatology etc...)

Our mission

We aim to deliver top-quality services and delivrables to clients, in a timely manner and with the greatest flexibility

Our values

Transparency, commitment to the projects, accuracy of the results and open communication are our core values


Our wealth of experience in biostatistics, with more than 20 years in the field, enables us to to support wide range of clinical projects for many pharmaceutical comapnies and CROs

Statistical programming

We offer the highest expertise in SAS® programming from our talented team enabling to support and answer any kind requests



- Protocol and study designs

- Power and sample size calculations

- Statistical analysis plans

- Analysis, reporting, and publications

- Exploratory analyses

- Data Monitoring Committee support

Statistical programming

- CDISC SDTM datasets

- CDISC ADaM datasets

- Programming of tables, listings and figures

- Define.xml

- Reviewers guides

- CDISC compliance reports


- Design

- CRO surveillance

- CDISC support

- Health Authority requests

- FDA/EMA regulatory activities

- Development of reporting tools (SAS®, .NET)

Contact information