CRO

For more than 30 years, we have been successfully advising our partners in the medical industry on the design and conduct of clinical trials with medical devices.

Our experience in studies of all risk classes according to EU MDR 2017/745, MPDG/MPG, and national EU regulations enables us to offer appropriate, solution-oriented options wherever questions arise.

Clinical studies are the foundation for successful medical innovations and therapies. Quality, reliability, reproducibility of clinical data, and cost considerations are today prerequisites for promising studies, especially in an international context.
The CE marking of medical devices is directly linked to the validity of data from clinical trials.
As a CRO, we offer practical, feasible, efficient, and professional services for these tasks of responsibility.
By strategically assigning key responsibility areas, we integrate expertise across all aspects of contract research. Our professional knowledge is continuously developed and strategically applied with a clear focus on achieving results – on this basis, even complex issues can be addressed with solid medical, scientific, and legal expertise.
Expert consulting offers planning security to our business partners and efficient resources allocation for the study conduct.
Thanks to our flexibility, we can respond quickly to new requirements and present well-considered concepts and practical solutions in a timely manner.