ÜTS Product Registration Consultancy

ÜTS Product Registration Consultancy: Professional Solution for Your Medical Devices and Cosmetics
Product Tracking System (ÜTS) is a system managed by the Turkish Medicines and Medical Devices Agency (TİTCK) and was created to ensure the tracking, inspection and legal compliance of medical devices and cosmetics. ÜTS product registration is a mandatory process for companies to legally launch their products on the market and this process must be completed completely.

However, the ÜTS registration process can be complex and time-consuming. Incorrect or incomplete applications can delay the entry of products into the market and cause serious commercial losses. This is where ÜTS product registration consultancy comes into play, helping companies complete the process quickly, without errors and in accordance with the legislation.

What is ÜTS Product Registration Consultancy?
ÜTS product registration consultancy is a professional service offered to register your medical devices and cosmetics in the ÜTS system in accordance with the legislation and to complete the TİTCK approval process smoothly.

Thanks to this consultancy service, all technical details, document controls and electronic signature transactions in the registration process of your products are managed by experts and the process is accelerated.

How Does the ÜTS Product Registration Process Work?
The ÜTS product registration process is an official procedure that includes certain stages. Since incorrect or incomplete applications may prolong the process, each step must be completed carefully.

1. Completing the Company Registration
In order to register a product in the ÜTS system, the company must first be registered in the ÜTS system. If the company registration has not been made yet, the ÜTS company registration must be completed as the first step.

2. Preparing Product Information and Entering it into the System
The products to be registered in the ÜTS;

Brand and model information,
Product class and category,
Manufacturer or importer information,
Technical documentation and label information,
CE certificate or other necessary certificates must be prepared completely.
At this stage, it is of great importance not to enter incomplete or incorrect information. ÜTS consultancy ensures that all documents are correct, complete and up-to-date during this process.

3. Regulatory Compliance Check
In order for products to be registered in the ÜTS, they must fully comply with the TİTCK legislation.

Compliance with the 2017/745 (MDR) and 2017/746 (IVDR) regulations for medical devices
Compliance with the Cosmetics Regulation for cosmetic products
Compliance with the Ministry of Health regulations for biocidal products
These controls are of critical importance in order to avoid any delays or rejections in the later stages.

4. Approval with Electronic Signature (e-Signature)
After the product registration process is completed, the authorized person must approve the application with an electronic signature (e-Signature). ÜTS consultancy service prevents loss of time by ensuring that the e-signature process is completed quickly and smoothly.

5. TİTCK Approval and Market Launch
After the ÜTS product registration process is successfully completed, the products can be officially launched on the market. As a result of the evaluation made by TİTCK, the approved products become active in the system and can be legally offered for sale.

Benefits of ÜTS Product Registration Consultancy
While the ÜTS registration process is mandatory for companies, incorrect or incomplete applications can prolong the process and lead to commercial losses. ÜTS product registration consultancy provides significant advantages to companies at this point:

✅ Time Saving and Fast Process Management
Thanks to the consultancy service, complete and correct applications are made, thus eliminating delays in the registration process. Your products are quickly launched to the market.

✅ Compliance with Legislation and Legal Assurance
By ensuring full compliance with TITCK and international legislation, the approval process of your applications progresses smoothly.

✅ Elimination of Error Risk
Registration processes are completed in the most accurate way by avoiding rejection or revision processes caused by incomplete or incorrect applications.

✅ Market Access and Increased Reliability
Products with completed ÜTS registration become legally sellable and marketable. This increases the reliability of your company and supports your commercial success.

✅ Continuous Support and Update Services
ÜTS system may be updated over time and additional document requests may occur. Thanks to the consultancy service, you can quickly adapt to changes in the system and keep your product records up to date.

Simplify Your Process with ÜTS Product Registration Consultancy!
ÜTS product registration process can be complex and time-consuming without professional support. However, by receiving expert consultancy service, you can speed up the process, minimize errors and launch your products without any problems.

🔹 Fast and reliable ÜTS registration process
🔹 Complete document and application management
🔹 Full compliance with legislation and legal assurance
🔹 Trouble-free progress with expert consultancy

📞 If you also want to get professional support for your ÜTS product registration processes, contact us now!