Unifarm University Consortium (Consorzio Universitario Unifarm, UNIFARM) was founded in Catania in 2002 by Filippo Drago, Professor of Pharmacology at the School of Medicine, University of Catania, in cooperation with the University of Catania and twelve major multinational pharmaceutical companies. In the same year the Research Centre in Clinical Pharmacology the first in Central...read more

UNIFARM is a CRO registered at  the Agenzia Italiana del Farmaco (Italian Authority for Drugs, AIFA), compliant with the requirements of the DM (Ministerial Decree) dated March 31, 2008 on clinical trials and therefore able to provide services such as: clinical study design; project management; preparation of study protocols and other regulatory documents; approval procedures...read more

UNIFARM has implemented a Quality System in line with national and international regulations to ensure high level of service and client satisfaction. Indeed, this is one of the main objectives of UNIFARM and is constantly pursued through the involvement of all the personnel in a quality process based on the assumption of individual responsibility, as well as through the implementation of systems and procedures...read more

Clinical Department

UNIFARM  cooperates with both  University and hospitals to perform clinical studies phase I-IV. In particular for bioequivalence studies UNIFAR signed an agreement with the Reparto Paganti ( ward for paying patients) of the Azienda Ospedaliera-Universitaria “Policlinico-Vittorio Emanuele” of Catania. The ward is well equipped and has the appropriate size to perform  clinical studies.

 
The following are available in the ward:
area for the registration and screening of volunteers;
area for hospitalization (8 beds with emergency devices);
recreational area;
toilets in each room;
pharmacy;
area for drug dispensing and samples collection
area for equipments (freezer -20°C and centrifuge) and for material disposal
archive;
emergency equipments and intensive care unit; 
medical and nursing staff.
 
All services are compliant with the International Conference of Harmonisation - Good Clinical Practice (ICH-GCP).
All services are compliant with the International Conference of Harmonisation - Good Clinical Practice (ICH-GCP).UNIFARM  cooperates with both  University and hospitals to perform clinical studies phase I-IV. In particular for bioequivalence studies UNIFAR signed an agreement with the Reparto Paganti ( ward for paying patients) of the Azienda Ospedaliera-Universitaria “Policlinico-Vittorio Emanuele” of Catania. The ward is well equipped and has the appropriate size to perform  clinical studies.
The following are available in the ward:
area for the registration and screening of volunteers;
area for hospitalization (8 beds with emergency devices);
recreational area;
toilets in each room;
pharmacy;
area for drug dispensing and samples collection
area for equipments (freezer -20°C and centrifuge) and for material disposal
archive;
emergency equipments and intensive care unit; 
medical and nursing staff.
 
All services are compliant with the International Conference of Harmonisation - Good Clinical Practice (ICH-GCP).

 

Unifarm è un Centro di Saggio (CdS) certificato dal Ministero della Salute,
in Buona Pratica di Laboratorio (BPL)