in various indications due to almost 25 years of CRO business in Central & Eastern Europe
Close relations to Universities, opinion leaders, research sites
and medical associations provide a fast access to specialists.
Prestudy visits and feasibility check, set-up of co-operation networks
between trial sites and external providers as e.g. local labs, X-ray-,
CT-, MRI- sites etc. Central laboratory services established in Prague, for all CEE and other countries, too.
Project manager or CRA supervisors perform site-by-site visits with
monitors, during the initiation phase of a clinical trial as well as throughout the
study. They discuss site-specific findings and conditions and lay
down what and how is to be followed up consistently.
Full service before, during and after the event: invitation, organization,
accommodation and travel, lectures in local language or in English,
GCP training and national provisions, information material