With more than 25 years of experience in the biotech & pharmaceutical industry, our activities relate to good Clinical Practices quality assurance phases i-iv applied worldwide.
We’ve experienced the development and performance of clinical trials across the world and the implementation of ICH GCP along with EU, FDA and country specific regulations.
We welcome new clients to partner with in the future challenges of conducting high quality clinical trials.
Don’t hesitate to contact us.
— Dag Tennerus, Founder