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WE CONDUCT CLINICAL RESEARCH IN ACCORDANCE WITH ICH-GCP,
LOCAL LAWS, EUROPEAN AND FDA LEGISLATION THROUGH BEING
A RELIABLE AND RESPONSIVE LINK BETWEEN SPONSOR, ETHICS
COMMITTEES, REGULATORY AUTHORITIES, SERVICE PROVIDERS
AND INVESTIGATORS.
We focus on our customers needs through commitment, punctuality
and flexibility, to achieve your project timelines and milestones.
We have been contracted to support clinical research for:
– LARGE PHARMACEUTICAL COMPANIES (TOP TEN)
We run national and participate in international registration, multi-center
studies for pharmaceutical companies who rank
among the top ten pharma companies in Europe, USA, Japan.
– BIOTECHNOLOGY COMPANIES
We organize early stage clinical trials.
– ONCOLOGIC STUDY GROUPS
We manage multi-center clinical trials in Eastern and Western Europe
LOCAL LAWS, EUROPEAN AND FDA LEGISLATION THROUGH BEING
A RELIABLE AND RESPONSIVE LINK BETWEEN SPONSOR, ETHICS
COMMITTEES, REGULATORY AUTHORITIES, SERVICE PROVIDERS
AND INVESTIGATORS.
We focus on our customers needs through commitment, punctuality
and flexibility, to achieve your project timelines and milestones.
We have been contracted to support clinical research for:
– LARGE PHARMACEUTICAL COMPANIES (TOP TEN)
We run national and participate in international registration, multi-center
studies for pharmaceutical companies who rank
among the top ten pharma companies in Europe, USA, Japan.
– BIOTECHNOLOGY COMPANIES
We organize early stage clinical trials.
– ONCOLOGIC STUDY GROUPS
We manage multi-center clinical trials in Eastern and Western Europe
| We deliver the highest quality according to global standards |
We give your project and your timelines highest priority |
| We have well training and experienced clinical research professionals | We guarantee focus on your project across all concerned countries and functions |
| We are a competent link between sponsor and investigator |
We have longstanding, tested and trustworthy partnerships |
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