Clinical Research
CIDAL offers services for Clinical Trials and Biomedical Research with various degrees of involvement and responsibility, which include participation as:
Contract Research Organization (CRO)
Represent sponsors, select study sites and monitor scientific, technical and regulatory aspects of a study.
Site Management Organization (SMO)
Identify, contract and supervise investigators and study coordinators; submit proposals to local ethics committees and health authorities; provide administrative and logistic support to investigational sites.
Combined CRO and SMO
Following strict guidelines and establishing firewalls between Clinical Research Assistants and Investigators / Site personnel.