Within the framework of development policy, define the clinical trial programme on the national level and supervise the whole process, from trial preparation through to writing the corresponding reports, with a view to product registration.
- Draw up protocols.
- Coordinate and check the action of the clinical research supervisors.
- Write study reports and publications on the trials.
- Handle administrative monitoring and check the budget allocated to the trials.
- Oversee compliance with the protocols by the investigators.