Coordination Center for Clinical Studies (KKS)

The core facility is service based. It provides clinical study support services: 1st study planning and initial consultation (pre-submission advice for clinical studies and medical research projects, guidance on study design, regulatory requirements, and funding opportunities in collaboration with research administration units); 2nd regulatory and administrative support (identification of additional requirements such as contracts and data protection, preparation for ethics committee submissions in compliance with applicable regulations and ethical standards, and review of clinical studies in collaboration with contract management teams); 3rd training and study management infrastructure (delivery of certified training on GCP and MPDG standards, and management of a central clinical study registry) Share on