vElaboration of projects (protocols), clinical files and research CRFs.
vPre-Clinical Phase Development
vLogistical control of the distribution of investigational products
vDevelopment of manual or electronic case report forms
vScientific and statistical consultancy
vSelections of Research Center Coordination and Researchers
vRegulatory process for ethic and legal approvals
vMonitoring, Coordination, Training, Management
vElaboration of final Reports, Articles and Pharmacovigilance
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