NAVIGATING TÜRKİYE’S LICENSING PROCESS WITH EXPERTISE

Trispera provides end-to-end support to international pharmaceutical companies aiming to register and launch their products in Türkiye. Our services cover the full scope of the licensing process, from pre-submission strategy to post-approval compliance—ensuring full alignment with local regulatory requirements and standards set by the Turkish Medicines and Medical Devices Agency (TİTCK).

We offer expert guidance in the preparation, submission, and follow-up of regulatory dossiers, while helping our partners interpret and navigate Türkiye’s complex regulatory environment. Our support includes tracking regulatory timelines, managing communications with local authorities, and assisting with the documentation required for marketing authorization applications.

Post-licensing, we continue to support our clients through processes such as renewals, variations, and ongoing regulatory reporting—ensuring continuous compliance with applicable laws and guidelines.

With deep experience in the Turkish pharmaceutical regulatory landscape and strong collaboration with key local stakeholders, Trispera is a reliable partner in streamlining your licensing journey—ethically, efficiently, and transparently.