SSIはCRC(治験コーディネーター)による質の高い治験支援を提供するSMOのリーディングカンパニーです。

WHO
WE ARE

What is SMO

What is SMO
Our Role and Function

We strive to be an indispensable partner to our clients by providing comprehensive clinical trial support in wide range of therapeutic areas.

SSI assists clinical trials at medical institutions as a Site Management Organization (SMO). We are able to leverage our extensive experience and expertise to provide our clients with a ‘one stop service’ in running a clinical trial, including general administrative tasks, and coordination of Institutional Review Board (IRB). We partner with various medical institutions throughout Japan, ranging from clinics to large hospitals. And, our support structure is able to handle a broad range of studies, including oncology, CNS, orphan and lifestyle diseases, as well as cutting-edge treatment such as regenerative medicine.

Role and Function of SMO in Clinical Trials

・We abide by the Pharmaceutical and Medical Device Act (PMD Act), GCP regulations, and other related guidelines when assisting clinical trials.
・We reduce the burden on doctors and medical staff by assisting them onsite with the clinical trials.

Role and Function of SMO in Clinical Trials