Project Management

  • Clinical trial planning oversight
  • Monitoring of strategy Development
  • Design and maintenance timeline expectations
  • Communicate with internal team members, the sponsor and other relevant subjects
  • Assurance of compliance with GCP and other regulations and guidelines
  • Preparation of progress and status reports
  • Adverse Events tracking and management
  • Internal and external regular meetings and communication, TCs
  • Monitoring
  • Efficient data flow
  • Clinical trial materials management
  • Ethics Committees and regulatory submission/approval tracking
  • Quality assurance
  • Audit Site preparation
  • GCP and trial-specific trainings
  • Consulting services

We deliver high quality services 

in the Czech and Slovak Republics.

We put our emphasis on quality, experience, credibility and flexibility.

We invite you to consider our services and to contact us to discuss your clinical trial and pharmaceutical needs.