EXPERTISE

• Phase I/ II/ PROOF OF CONCEPT patient trials, in own state-of-the-art research clinics
• Project Management/Study Coordination
• Regulatory Affairs (dossier preparation and submission to HA/EC, import/export of study medication etc.)
• Scientific advice for protocol development (medical considerations on all aspects of protocol development e.g. in/exclusion criteria, study design, logistical aspects etc.)

Satellite services via ARENSIA qualified vendors for medical writing, data management, biostatistics, central laboratory and bio-analytical services can be recommended.

We collaborate with the leading pharmaceutical companies worldwide, as well as with numerous biotechnology companies.

Global and mid-sized full-service Clinical Research Organizations utilize ARENSIA's services to conduct early phase clinical trials involving patients. This approach allows Pharmaceutical companies that are bound by global outsourcing agreements with selected full-service CRO vendors to use ARENSIA’s expertise and speed.

By involving ARENSIA, our research partners have considerably benefited in reducing recruitment periods, and the overall number of involved clinical trials sites/countries in a range of studies. This translates into major financial savings for the total project lifecycle.