CTC Cologne offers medical professionals, researchers and companies as a research partner tailor-made solutions with the corresponding infrastructure.for the design and implementation of their clinical studies

The range of services for the management of clinical studies depends on your wishes and the respective contractual agreements. It ranges from targeted support in individual areas of study planning, preparation, implementation or completion to complete study management. This can include the whole spectrum from the preparation of the study protocol, the patient informed consent forms to report and publication writing as well as other regulatory documents.

Generally we as CTC Cologne assume the role of a cooperation partner. The individual servicess comprise the areas shown below. Strict quality criteria are applied in the planning and implementation of the clinical trials we are responsible for, which are based on the principles of the Declaration of Helsinki and GCP.