Services in the Field of
Clinical Research  

Excellent planning and coordination

The systematic organization of clinical trials is fundamental to their smooth performance! Maintaining an overview in the “regulatory jungle” and meeting the high regulatory requirements requires detailed planning and coordination.

With the help of TETEC AG's comprehensive expertise and many years of experience, we can support you in the creation of study designs and the professional implementation of your clinical programs - with the aim of avoiding errors, saving costs and, above all, gaining valuable time in the approval process.

20 years of experience in clinical trials

Our clinical department has more than 20 years of experience in conducting clinical studies in various indication areas (randomized, controlled clinical trials according to GCP, phase I to III, as well as non-interventional studies). Based on this extensive expertise, we are also happy to coordinate external clinical CROs and logistics service providers.

Our in-house regulatory department is committed to support you in the preparation of CMC documentation for the submission of the intended applications. Our experienced colleagues maintain long-term relationships and contacts with relevant consultants and authorities.

Your contact person for our CDMO services

Do you have questions about our CDMO services, or would you like to learn more about our portfolio? Our CDMO experts are at your disposal. We look forward to talking with you.

Dr. Christian Ebel
Head of Business Development
Aspenhaustraße 18
72770 Reutlingen