Site Identification

We are fully aware that the ultimate success of a study is linked to the selection of appropriate, qualified and productive sites, which is why we put a particular emphasis on site identification.

We can take full responsibility for the initial selection of sites or combine your own database with our lists.

Our process includes a detailed evaluation of the following aspects:

• Past history of clinical study/research involvement
• Investigator competencies and experience in clinical trials and health research studies
• Availability of co-investigators and research team
• Team workload
• Ongoing competing projects
• Training of site staff in ICH-GCP, other regulatory requirements and local procedures
• Site facilities and equipment
• Recruitment potential

Wherever possible we also maintain a list of backup sites in an operational state on stand-by that can be quickly initiated if additional sites or site replacement are required.