The ISS (Investigator Sponsored Studies)


You can grant to us the role of promoter and we will take care of all the obligations linked with insurance and the electronic transmissions of SUSAR. We will unburden the investigators of all the regulations, pharmacovigilance, medical writing, biometry, we can assure the monitoring aligned with the other CRA.

We will keep you informed to the nearest Euro of how your grant is being used.
You will have an up-to-date schedule. We will take care of the results publication and assure the follow-up process with the trustee authorities.

The Investigators often ask for these studies: We manage many of them at any given "t" time .

They can originate from cooperative groups, auto-sufficient rules and financers of clinical research often from biometry and other supporters.
You can ask for outside monitoring for these studies. For an audit or inspection, it is sometimes best that an organisation without any potential conflicts of interest follows the study. Alternatively, you can ask our Clinical Research Technicians to help the Investigators include more subjects.

They can come from more modest or less well equipped teams. Therefore supplying you with a classic subcontract.

.