Clinical Monitoring
Typically we provide clinical monitoring services for North American and European (Western, Central and Eastern Europe) sites, in addition we have monitored sites in South America and Australia.
Cmed CS utilizes a combination of in-house and field-based personnel to monitor our clients’ clinical research studies. The use of independent clinical professionals gives flexibility from a logistical perspective in terms of monitor location, adequate and appropriate resourcing (with adaptability around the peaks and troughs of clinical study activity). Ultimately it is a streamlined approach to clinical monitoring – so you get the most from your budget.
Timaeus, our advanced clinical data capture and management system, uniquely allows the project team to have real time access to their data and trial status. Clinical teams, including management and monitoring personnel, are able to access study clinical data, trial progress, metrics, and reports. A strong, cross-functional inter-departmental working relationship is a key element, as Cmed CS data managers review/ raise queries before CRAs visit each site.
The Cmed CS model uses CRA time more efficiently than traditional models and by sourcing CRAs in a different way Cmed CS focuses on completing each project and does not see monitoring as a commercial exercise in CRA utilisation.
