For more than 10 years, our company succeeds in advising our partners in the pharmaceutical industry regarding conception and conducting of clinical trials. Our wide study experience according to Medical Device Regulations for all risk categories enables us suggesting adequate solutions to our partners whenever and wherever necessary.
Quality, reliability, reproducibility of clinical data and the economic cost aspects are all necessary requirements for successful trials, especially compared to international standards.
Targeted certification of medical devices for CE approved products are based on valid data from clinical trials.
For this reason, we can offer the research industry practically orientated, efficient and professional service by covering all necessary aspects of a clinical trial.
By offering exceptionally well-trained team members we can cover all areas of scientific research.
By specific placing of our area of responsibility, we not only improve our professional expertise and knowledge, but are able to allocate purposefully. Therefore all medical, scientific or legal matters can be solved immediately and in house.
We offer our business partners informed advice and reliability, which positively influences the conduct of trials.
Our flexibility permits us to present even more complex concepts and solutions quickly.
