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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
 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