NAVIGATING LOCAL REQUIREMENTS WITH CLARITY AND CONFIDENCE

Türkiye offers a dynamic environment for clinical research with a growing infrastructure, experienced investigators, and increasing patient engagement. However, successfully initiating and managing clinical studies in Türkiye requires a thorough understanding of local regulatory frameworks and ethical standards.

Trispera provides expert guidance to sponsors, CROs, and investigators throughout the clinical research lifecycle—from protocol development to regulatory submissions, site selection, ethics committee approvals, and post-trial obligations.

With up-to-date knowledge of the guidelines issued by the Turkish Medicines and Medical Devices Agency (TİTCK) and the Ministry of Health, we ensure that your clinical operations align with national regulations, timelines, and documentation expectations.

By partnering with Trispera, you gain a reliable local ally to help you navigate Türkiye’s clinical research ecosystem with precision and peace of mind.