ERGOMED's approach to Site Management ensures effective patient recruitment reducing time and cost of clinical trials.

ERGOMED’s position as the leader in the successful integration of Site Management Capabilities into full Clinical Development Services is very highly regarded by sponsors as well as investigators. Optimal investigator site contribution is ensured by combining good patient recruitment with high quality data collection and assistance to investigators with their many administrative and logistical responsibilities including scheduling of patient visits, shipment of blood samples etc.

ERGOMED’s Study Site Coordinators work strictly in accordance with ICH/GCP and completely independently of CRAs and PMs; they follow their own SOPs and have a separate line management and reporting structure.

SSC support to investigators results in:

• Faster recruitment
• More patients per site
• Enhanced data quality
• More timely data entry
• Fewer data queries
• Better compliance to GCP

Additional information regarding Site Management service.