Site Management Organization
Planning, which is one of the most important elements of an effective clinical study, is the starting set of our most.MORE INFORMATION »
Regulatory Authority Submission Services
In order to initiate the clinical trial in timely manner, we manage the approval processes smoothly with our trained, equipped and experienced experienced teammates.MORE INFORMATION »
Clinical Trial Management
We perform all monitoring and termination activities studiously according to the ICH-GCP, 2017/745 MDR, ISO 14155 and MDCG guidelines.MORE INFORMATION »
SUPPORT AND CONSULTING
Our Expert Teams
Our experienced, stable and innovative task force is the key to the effective management of our commercial activities and company processes.
We are proud to contribute to our efforts to build and maintain trust with high customer satisfaction and long-term partnerships.
WHAT DO YOU NEED?
Contact Us
And identify your position in the sector!
