Non-Interventional Studies (NIS) are performed for approved drugs within the standard therapy.
Usually, these studies are intended for the documentation of the use of a drug under "field conditions", i.e.
without the "experimental bias" of clinical studies. As such studies are initiated to expand the safety experience
and patient compliance on a drug, large sample sizes will become necessary. This implies specific logistic
problems for clinical operations.
SIRO has gained wide experience in longitudinal as well in cross-sectional studies in various
indications. Our experienced team is able to take over document, administrative and clinical grant management,
even in very large NIS.