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.