Full services multinational CRO with high expertise in:
- Regulatory and Pharmacovigilance
- Trial Management and Monitoring
- Data Management
- IP Management
Development and supervision of dossiers and documentation regarding national and European authorisation procedures for medicinal products. Find out more.
Development and management of all clinical trial phases, which are performed by the Consortium both as a Sponsor and as a Contract Research Organisation (CRO). Find out more.
Educational activities addressed to public bodies, research institutes and private companies, also within CME programmes. Find out more.
On 28 January, 2020, the event “IlluminAutismo, SPASD project and inclusive education” took place at the Liceo "Enrico Fermi" of Bari. The meeting involved different professionals involved in the school an teaching framework such as teachers, [...]
SAVE THE DATE. Nuovo Webinar EUCROF intitolato “The Patient Centricity Effect – How it benefits Patients, Sites and Sponsors – Practical Cases from Paediatric Studies”. 25 Febbraio 2020
The Events&Training Working Group of EUCROF (European CRO Federation)...