KKS will gladly take over the entire project management of clinical studies or just specific sub-areas, as required.
In addition to advising on study planning, this can also include assisting with or taking over the following areas:
- Submissions to Ethics Committee and authorities (Regulatory Affairs)
- Drawing up the Responsibility List
- Compiling study documentation and reports (Medical Writing)
- Project preparation and monitoring of project flow
- ICH-GCP-compliant monitoring for Quality Control
- Communications, support, and supervision of study sites
More information is available under the other service sections.