REGULATORY SERVICES
Farefarma S.r.l. offers a complete range of experimental and regulatory services for the registration of medicines.
We support our clients in every phase of their project, both in the entire process and in individual specific activities, from the drafting of study protocols to the conduct and monitoring of research, up to the analysis of data and the preparation of documentation and reports.
Our Regulatory team has consolidated experience in drafting expertises for veterinary drug‘s registration dossiers, evaluation of environmental risks and user‘s risks according to the current guidelines. We can assist you in preparation of the dossier application.
We guarantee continuous updating on national and EU regulations, offering technical and professional advice for complete and compliant project management.