Excellent planning and coordination
The systematic organization of clinical studies is fundamental to their success because navigating the “regulatory jungle” requires detailed planning and coordination.
With 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 development programs – with the aim of avoiding errors, saving costs and, above all, gaining valuable time in the authorisation process.
20 years of experience in clinical trials
Our clinical department has more than 20 years of experience of conducting clinical studies in a range of indications (randomized, controlled clinical trials according to GCP, phases I to III, as well as non-interventional studies). Based on this extensive expertise, we will also be happy to coordinate external clinical CROs and logistics service providers.
Our in-house authorization department will be committed to supporting you in the preparation of CMC documentation for the submission of the necessary applications. Our experienced employees maintain long-term relationships and contacts with the relevant consultants and regulatory 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 will be happy to help. We look forward to meeting your CDMO needs.