About us

Leading CRO in Poland providing professional
and tailored solutions for pharmaceutical,
biotechnology, and medical industry.

Biostat was founded in 2005 to provide high-quality, comprehensive services in clinical trials, non-interventional studies, biostatistics, eCRF system, telemedicine, patient support and R&D services, data collection and medical software solutions.
The company has since grown to be one of the largest CROs in Poland. The company employs more than 100 people in many locations and across Poland.

In 2019 Biostat has been given the official title of R&D Centre by the Polish Ministry of Economic Development and Technology.
years of business
and scientific experience
projects conducted within
our professional service
employees including engineers,
analysts, biotechnologist,
managers, IT innovators
collaboration with Polish
and international Sponsors
publications with
Biostat assistance
0 500+
consulting services

Management Team

People are the greatest strength of BioStat® and it is their expert knowledge that the BioStat ® brand value is based on. A specialized team of project managers, statisticians, programmers, monitors, managers with a background in medicine and biology, biotechnology, bioengineering, chemistry, biostatistics with many years of experience in designing and developing systems, applications, studies.
Rafał Piszczek
Chairman & Chief Executive Officer

Dr inż. Ewa Tkocz-Piszczek

Vice Chairman

Edyta Klemba

Pharma Division Director

Dr Marian Płaszczyca

Head of the Statistics Unit

Szymon Błąkała

Head of IT department

Dr Monika Jaremków

Resarch Director

Wacław Wrana

Development Director

Bartosz Olcha

Research Director



Implementing scientific knowledge into business.

That’s our advantage Our mission has always been research and development in the field of healthcare and clinical data collection.

Biostat CRO service offers full coverage of clinical evidence collection process for medicinal products and medical devices, together with required clinical and scientific expertise, applicable study tools, legal and administrative support.

We provide Phase I to Phase IV clinical development services and bioequivalence, for medical products and medical devices. With expertise of all major therapeutic areas, we deliver the an high-experienced team, combined with the fast responsiveness, and client focus.


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