EXCO will assume responsibility for all the phases of a clinical trial and will observe stringent methodical, ethical and regulatory requirements.

• Feasibility studies and concept analyses
• Validation of ethical innocuousness
• Trial design
• Planning as per IVDD/Medical Devices Act and implementation
• Recruitment and supervision of test centres
• Clinical tests
• Clinical analysis
• Trial monitoring
• Supervision and analysis
• Documentation

In our coordinating capacity as project manager or monitor, we will ensure that all project work is carried out in line with objectives, in a structured manner, and reliably. We will collaborate closely with colleagues in the relevant specialist department with regard to budget negotiation and medication.

EXCO monitors the observance of general legal conditions, good clinical practice guidelines (ICH-GCP), the German Acts on Pharmaceuticals and Medical Devices, and the test and monitoring plan. By defining appropriate criteria and procedures, we ensure that the trial meets internationally recognised quality standards.

EXCO creates synergies for the quick and cost-effective implementation of clinical trials in a way that is tailored to the needs of your customers. Existing resources are consolidated and enhanced. They optimise the flow and quality of your clinical trial.