International experience in the preparation of regulatory procedures

Arcus Pharma Consult  regulatory department has highly skilled personnel,  specialized in regulatory procedures in strict  accordance to the ICH-GCP (2001/20/EC) and their adaptations in individual countries.

Arcus Pharma Consult will be responsible for all phases needed to obtain regulatory permission for the study, from filing the application to the relevant authorities to paying the compensation due to the EC, including the final contract.

The Arcus Pharma Consult Regulatory Deptartment is able to ensure  competence and knowledge, within the existing regulations in each individual country  in order to ensure, in the shortest possible time, a successful approval  of the study