I'm interested

CreaBio can take over all project steps from protocol conception, to full study execution until clinical trial reporting. These tasks include the protocol writing and review, obtaining study authorization from Ethic Committees and Countries Agencies, study equipment supply, monitoring, quality audit and adverse events reporting when required.

CreaBio ensures data management and data analysis with statistical report.

CreaBio can provide medical writing in French and English languages, manuscript preparation for submission in peer reviewed journals.

CreaBio offers services in Europe and USA through RCTS and PSN network of International CRO.