Our services include:

• Clinical trial monitoring in Central Eastern Europe.
  
  
• Investigator Meetings.
  
  
• Conduct, monitoring and management of Phase I-IV and post-marketing surveillance in different indications.
  
  
• Effective assistance in selecting trial centres, regulatory and EC approvals and other initiation activities (including medical translations).
  
  
• Organisation of start-up/investigator meetings under price-convenient conditions.
  
  
• GCP training for your research personnel and investigators.
  
  
• Provision of contract staff from our large database of free-lancers.
  
  
• Medical writing and translations.