Driving successful
Investigator Initiated Studies
At Clicebo, we ensure compliance with all legal and regulatory requirements, keeping the conduct of the studies undertaken in accordance with all the applicable laws and regulations.
We pledge our accountability for the initiation, management, and finance set-up of the clinical investigation, data collection, and processing, biostatistics, and data monitoring throughout the lifecycle of the study.
Investigator Initiated Studies (IIS) are clinical studies initiated and managed by a nonpharmaceutical company researcher/s who could be an individual investigator, an institution or a group of institutions, a collaborative study group, or a cooperative group.
Benefits of
Investigator Initiated Studies
Data generated in
real world setting
No intervention
from industry
Cost
effective
Flexibility
in design