•     Feasibility studies-Site Selection
•     Submission to Ethics Committees and Regulatory Authorities
•     Pre-Study Site Visits, Investigator assessments
•     Site Initiation, Interim Monitoring and Close-Out Visits
•     Complete monitoring activities associated with Phase I - IV Clinical Research Trials
•     Training of the clinical study team
•     Training of Junior/Senior CRA's
•     Quality Site Visits
•     Project Management
•     Medical Writing
•     Providing scientific information to key opinion leaders
•     Using own network of professionals for your capacity demands
Clinical Research Assist - © 2012 - DOEN! Webontwerp