ENSURING PATIENT SAFETY THROUGH CONTINUOUS RISK MANAGEMENT

Pharmacovigilance is a key regulatory and ethical obligation in the pharmaceutical lifecycle. At Trispera, we coordinate all necessary processes in collaboration with authorized local PV partners to ensure seamless and compliant operations in Türkiye.

Our role includes identifying and liaising with licensed pharmacovigilance service providers, setting up appropriate adverse event reporting mechanisms, and ensuring that all safety-related activities meet the standards of the Turkish Medicines and Medical Devices Agency (TİTCK).

In cases of audits or inspections, we support our partners by facilitating documentation flow, coordinating with relevant stakeholders, and ensuring that all regulatory expectations are met in a timely and transparent manner. Through this coordinated approach, we help international pharmaceutical companies establish and maintain a robust PV presence in Türkiye without the need to manage these processes directly.