As you know, the Turkish Medicines and Medical Devices Agency (TİTCK) had given the relevant companies until May 31, 2013, to update all information and documents related to products registered in the TİTUBB system. Due to the expiration of this deadline, the announcement published by TİTCK is attached.
As can be seen from the announcement;
As of the end of the day on May 31, 2013, documents and related products that have expired will not be displayed in password-free inquiries.
If the production or import of a product registered in the TİTUBB system has been stopped and the validity period of the product's documentation has expired, the relevant manufacturer/importer companies must apply to the Turkish Medicines and Medical Devices Agency with the attached petition by June 17, 2013. In this case, the products will remain brown in the system for 90 (ninety) days starting from June 1, 2013.
Manufacturers/importers whose certificates and related products will expire after June 17, 2013, must submit a petition to TİTCK (Turkish Medicines and Medical Devices Agency) ensuring it reaches them by the end of business on the certificate's expiration date.
If no application is submitted, or if the submitted application does not conform to the published and attached sample, the relevant documents will be rejected on the next business day, and the related products will be moved to a new status.
The announcement states that there is no objection to purchasing a product whose documentation has expired, provided that the purchasing authorities verify whether the product was manufactured within the validity period of the documentation.
For products whose document validity period has expired, if the production date falls within the document's validity period, it is stated that the goods must be received within 90 (ninety) days after the document's expiration date.
If the product's manufacturing date and the validity period of the documentation have expired, the product should not be sold until it is registered with TİTUBB with new documentation.
Instructions on how to prepare the application file are included in the attached announcement, and a sample application form is also provided.
Best regards,
Medical Industry Cluster
