Project Management of Clinical Studies

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.