CIC 1417 can help or support the various stages of biomedical research
from upstream of the trial to the end of the trial
01.
Search for funding
02.
Drafting of study documents
03.
Coordination and monitoring of research in accordance with Good Clinical Practices
04.
Recruitment of research participants
05.
Interface work with biology laboratories
06.
Data exploitation and analysis in collaboration with the bio-statistics service
07.
Writing of study reports and scientific publications