On September 24, 2021 Turkish Ministry of Trade amended the Customs Regulation (“Regulation“). The amendments to the Regulation introduced a simplified procedure of “permitted consignor authorization” for transit regimes and clarified the scope of the crimes relevant persons must not have a final conviction of to open a temporary storage site or a bonded warehouse. The Ministry of Trade also regulated the transition process regarding permitted consignor authorization and site authorizations granted prior to the subject amendment within the scope of the Regulation on Facilitation of Customs Procedures.
The Turkish Medicine and Medical Devices Authority (TİTCK) published a critical announcement covering the topic of new practices for the registration and evaluation process of medical devices post-Brexit.
The Turkish Medicine and Medical Devices Authority (TİTCK) published two announcements covering critical topics on certain procedures concerning the Product Tracking System (ÜTS).
The Turkish Medicine and Medical Devices Agency (TİTCK) published the Application Guidelines for Electronic Scientific Meetings and Electronic Product Promotion Meetings (Guidelines) based on the Regulation on Promotion of Pharmaceuticals (Regulation). The Guidelines provide detailed explanations on electronic applications made to the TİTCK by relevant companies (e.g. marketing authorization holders) for scientific meetings and electronic product promotion meetings.
Further to the amendments to the Presidential Decree published in the Official Gazette No. 30887 on 13 September 2019, “biocidal products that directly come in contact with the human body (Product Type-1 and Product Type-19)” are now under the governance and supervision of the TİTCK. The licensing of biocidal products will be handled by the Cosmetic Products Department under the TİTCK. Accordingly, the TİTCK added ‘biocidal’ under the “Activity Areas” on its official website. The TİTCK’s announcement is available here (in Turkish).