Experts of GCP-Service International

Our excellence is your success. The expertise of the GCP-Service team in different types of clinical studies is one of our key values we provide to our clients. Our focus on agile small to midsize clients requires a special mindset of our experts which we develop and improve since the foundation of GCP-Service. The involvement of our experts ensures that the conduct of a huge variation of clinical studies, with its different study designs, objectives, products, medical areas in several geographical regions reach the goal. The fact that our experts work hand in hand to smooth the entire development process is unique in the CRO world. We are proud to introduce our pleasant expert team responsible for the cost-effective conduct of your studies as professionals and as humans:

Board of Directors


Andreas Beust PhD

Expert for Centralized Statistical Monitoring

Benjamin Tsiflidis

Expert for TMF & Document Management

Marcel Müller

Expert for Regulatory Submissions of Medical Device & Drug Studies

Dennis Neuschwander

Expert for Biostatistical Trial Planning

Marco Schwarzer PhD

Expert for Interface Management

Marion Gruenhagen

Expert for Training and Competence Management

Petra Stepankova

Expert for Quality Assurance

Sebastian Fessel PhD

Expert for electronic Patient Reported Outcome (ePRO)

Thomas Kissner

Expert for Data Management and Electronic Data Capture

Process/System experts


Jiří Paseka MD

Expert for Central and Eastern Europe

Andreas Grund PhD

Expert for International Project Management

Medical Device Consultancy Task Force Group

The goal of this Group is to help medical device manufactures with preparation to both the new Medical Device Regulation (MDR) and the new In Vitro Diagnostic Regulation (IVDR). We want to help companies to bring light into the dark. The Task Force Group works closely with our International Advisory Board that assures medical expertise truly throughout all therapeutic areas. Our multifunctional team can support you with:

– Development of a study design that proves the performance and safety of your product
– The sample size calculation to collect robust data
– Preparing an investigational plan
– Train your staff in the conduct of clinical trials with medical devices
– The selection of reliable investigators and cost-effective countries
– Preparing Clinical Evaluations
– Regulatory consultancy
– All other tasks which might help you to bring your product to the market.

Regional experts


Cordula Lühmann,

Belgium, Netherlands

Annelies Weyn PhD,


Aicha Boudhar,

Czech Republic, Slovakia, Hungary

Lenka Lupinkova,

Romania, Bulgaria

Andrei Stoicescu,

Turkey, Greece, Cyprus

Andreas Moschos,

North America

Miganush Stepanians,


Angela Conway,


Noga Brunicki,

Baltics, Ukraine, Georgia, Russia

Audrius Sveikata,

Spain, Portugal, Italty

Alfonso García Cañamaque,

Australia, New Zealand

Robin Hansen / Anne De Luca,