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Services for clinical trials:
- drawing up protocols and research documentation,
- organizing, monitoring, administration and management of international multi-center Phase I-IV clinical trials,
- comprehensive coordination of epidemiological and observational studies (from study planning to preparation of the final report),
- medical advisory service regarding programme planning, possibilities and solving medical difficulties as they occur,
- quality supervision, audit services at centres and for vendors,
- clinical research data management,
- statistical analysis,
- creation of clinical research reports.
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