CECOG provides full service for phase I-III clinical trials with particular expertise in Central and Southeastern Europe where CECOG has a broad net of contacts with academic centers and commands highest expertise for the implementation of clinical trials and rapid patient recruitment via these services:
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- Scientific advice and support
- Close cooperation with partners
- Involvement of international advisory board (optional)
- Study feasibility assessment
- Design and plan of clinical trials
- Site selection
- Clinical trial logistics
- Submission to EC and MoH
- Site monitoring
- Project Management
- Data Management, Biostatistics
We have been providing support for Pharma and Biotech industries for over 20 years. In cooperation with dedicated local partners we can provide high quality performance at more than 150 academic sites in 23 countries. By following GCP-ICH guidelines, SOP´s and international and national regulations we deliver high quality results of clinical trial. CECOG offers an extensive portfolio of services which can be customized to meet the individual needs of each client.