Operational guidance grounded in official sources, with review dates, product scope and direct regulatory citations.
Map a product import routeWho the importer of record is, which responsibilities cannot be delegated and how the matrix is built. The responsibility map of the import chain.
Read sourced guidanceWhich GTİP lines cover centrifuges and analysers, how CE and communiqué controls work for laboratory equipment, and why the equipment-versus-consumable split matters.
Read sourced guidanceWhich document chain does commercial phone import require? Surveillance, CE control, IMEI registration and Turkish-language requirements in one file.
Read sourced guidanceIs the kit an IVD, RUO or a chemical? Which regulatory regime the intended-use claim triggers, how the GTİP is chosen and how the import file is built.
Read sourced guidanceHow communiqué 2026/16 inspects medical device imports, which documents TAREKS requests and how ÜTS registration ties into customs. The annual control frame.
Read sourced guidanceWhich permit chain governs investigational medicinal product import, which document customs asks for, and what depot and labelling require. The end-to-end guide to IMP supply.
Read sourced guidanceHow to prepare a TAREKS conformity declaration, which documents to upload and which routes the risk analysis opens. Evidence, risk and timing before the customs declaration.
Read sourced guidanceTariff classification drives every import control step. This guide explains how to build a defensible classification file, step by step.
Read sourced guidanceWhat an audit trail records, how long archives are kept and how the annual communiqué change flows into operations. The records and change management guide.
Read sourced guidance