Advice and Information for Investigators and Sponsors
ItaCRIN can help Italian investigators and sponsors in preparing multinational clinical projects involving scientific partners from ECRIN Members and Observers countries, and also other countries.
As first step, the proposal has to be submitted to the ItaCRIN EuCo and then evaluated by the ECRIN Collaboration Committee for its approval. The ItaCRIN’s involvement in proposal preparation depends on its role. While information may be freely provided to all, ItaCRIN can:
Once the investigator/sponsor has identified an appropriate funding opportunity for her/his proposal, ECRIN can provide advice and information on:
It is recommended to contact ECRIN as soon as possible for maximum impact
The goal of this unique service is to improve the quality of multinational clinical proposals to be submitted for EU funding. This is achieved through early support on the protocol and the logistical/operational aspects of project design.
How It Works
The principal investigator (PI) submits a short study synopsis to the ECRIN EuCo in his/her country. ECRIN’s Scientific Board provides independent methodological consulting on the protocol, while ECRIN’s EuCos help on issues such as work package organization.
EoB is a service reserved for ECRIN Member Countries and can only be used for multinational projects involving at least two Member or Observer Countries.
How to apply
Learn more: www.ecrin.org/activities/ecrin-on-board