We partner with Sponsors, Manufacturers, Biotech Organizations, and CROs. Although the majority of clinical trials conducted in Europe involve west countries, the number of trials is increasing in Central and Eastern European countries and our benefits are related to this through:
- our Central European location,
- staff experience on GMP, GCP, and GDP, run with the EU regulation
This can be one of the best fitting choices for studies:
- conducted mainly in CEE & EU region and its logistic supplier is desired to bring closer
- requiring flexible and quickly available capacity on clinical labelling and IP distribution services
- requiring sub-contracted local depot in order to store and distribute clinical supplies within the EU.