- Clinical Trial Management
- Site monitoring
- Project management
- International project management
- Contracting
- Regulatory Affairs (Hungary, UK)
- Country feasibility
- Site selection
- Organization of investigator meeting
- QA Services
- Trial quality management and auditing
- Audit and inspection preparation
- International rescue monitoring
- Risk based trial management plan
- Independent medical interpretation at audits and inspections
- Medical Writing
- Medical device clinical evaluation
- Study protocol
- Investigator’s Brocuhe
- Electronic Case Report Form
- Patient Informed Consent Form
- Development safety update report
- Interim analysis report
- Clinical study report
- Monitoring and risk based monitoring plans