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.

Main activities

• 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.