We provide centralized external imaging support when study centers lack the necessary facilities. It is possible to perform a sample imaging for assessing the quality of imaging. Within our imaging services, our radiologist with clinical research experience can provide RECIST reporting, particularly requested in oncology studies. We are preparing the necessary software to facilitate the imaging evaluation and reporting process electronically.
Medical equipment requested by the supporter is rented for flexible durations specific to the study, calibrated, delivered to the centers under appropriate conditions, and their subsequent regular maintenance is conducted.
Managed by our IKU (GCP) certified medical translator, our experienced translation team ensures all documents related to the study, including PROs, are translated and prepared in accordance with country regulations. We support the smooth progression of authority compliance processes. Through our linguistic validation service, we adapt PROs to study objectives. As part of our services, we localize global documents like Master ICF to suit local conditions during the translation process.
Feasibility visits are made to centers or as defined by us according to the supporter's request, with Principal Investigators determined by the supporters. The verification of center facilities is ensured through remote or on-site visits. After evaluating the suitability of the center in line with the supporter's requests and protocol requirements, a detailed report is presented to the supporter.
We translate the inclusion/exclusion criteria of protocols and design them in a desktop-friendly format. After getting your approval and preparing for printing, we ensure they are directed to the centers. This service, often provided upon the request of the Principal Investigator and with the permission of the supporter, can be applied to many types of documents in clinical trials and various materials can be supported.
Especially in studies where it is difficult to find volunteers due to the criteria in the protocol or in rare diseases, the identification of patients suitable for the protocol and their referral to the centers where the study is conducted is ensured after our medical director reviews their suitability to the criteria. With the support of our wide professional network, including many healthcare organizations and physicians, and our lawyer proficient in the KVKK process, we support the volunteer registration process with a qualified team.
FACILITY MANAGEMENT (CRO) SERVICES