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- Participating in the selecting of facilities for carrying out clinical trials.
- Monitoring the progress of clinical trials, supervising compliance with the defined procedure by the investigators.
- Responsibility for reviewing the accuracy and data processing.
- Communicating with the regulatory bodies and other institutions.
- Preparing documents for the National Institute for Drug Control (NIDC) and the European Commission (EC).
- Submitting regular reports on the progress of studies.
