• HOME
  • SERVICES
    • Medical Device Registration with the Turkish Ministry of Health (MoH) National Database
    • Healthcare Market Research for Medical Devices
    • Regulatory Compliance Consultancy for MDR and IVDR
    • In-country Representation as Registration Holder for Medical Devices
    • Consultancy for Turkish Medical Device Manufacturers expanding Internationally
  • ABOUT
  • CONTACT US
  • HOME
  • SERVICES
    • Medical Device Registration with the Turkish Ministry of Health (MoH) National Database
    • Healthcare Market Research for Medical Devices
    • Regulatory Compliance Consultancy for MDR and IVDR
    • In-country Representation as Registration Holder for Medical Devices
    • Consultancy for Turkish Medical Device Manufacturers expanding Internationally
  • ABOUT
  • CONTACT US

Medical Device Registration with the Turkish Ministry of Health (MoH) National Database

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Regulatory Compliance Consultancy for MDR and IVDR

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Healthcare Market Research for Medical Devices

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SERVICES

Medical Device Registration with the Turkish Ministry of Health (MoH) National Database

We utilize years of hands-on experience to ensure our clients to get their products to market as efficiently as possible. We can compile, submit, and manage all your device registrations  and all post-registration, follow-up processes via "Product Tracking  System (UTS)" Our experienced consultants can review your documents, register your medical device or IVD, as required and respond to any questions or concerns from the Competent Authorities.


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Healthcare Market Research for Medical Devices

For the past four years, Ardis has been supporting medical device and IVD companies with market entry strategies in Turkiye. Our services include identifying, screening, and engaging potential distributors through targeted research and interviews, providing companies with essential insights and connections to establish a strong market presence.


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Regulatory Compliance Consultancy for MDR and IVDR

Ardis provides its partners with comprehensive guidance on Turkish regulatory requirements for medical devices. We offer consulting services to help our customers understand the operational procedures of regulatory bodies in Turkey and the classification criteria for medical devices, ensuring smooth and compliant market entry.


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In-country Representation as Registration Holder for Medical Devices

Medical devices intended to be sold in Turkey must be registered either through a local office or an authorized representative incorporated in the country Foreign manufacturers without a presence in Turkey need a local representative to fulfill this requirement. Ardis, as an in-country representative, holds the registration on behalf of foreign companies and manages all necessary procedures with Turkish authorities.

 

Key requirements include:

 

1) All medical devices must be registered with the MoH in the  UTS (Product Tracking System ) and registrations and notifications  must be made to TITUBB (Turkiye Drugs and Medical Devices National Database).

2) A local representative, known as the "Registration Holder," must submit UTS registrations.

3) The local representative must be a registered entity in Turkey and must have a company registration in the EBS  (Electronic Application System). 


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Consultancy for Turkish Medical Device Manufacturers expanding Internationally

Ardis  enables medical manufacturers in Turkey to leverage the expertise of  external partners to grow their businesses and bring industry-changing solutions to the market. We have been supporting local manufactures in Euorope with answering questions on Key Opinion Leader (KOL) searches and interviews, logistics issues and other topics before they can actually start selling in a market. 


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ABOUT US

Ardis Consulting delivers specialized consultancy services across the healthcare sector with a team that has over 20 years of experience in their fields.Ardis Consulting delivers specialized consultancy services across the healthcare sector with a team that has over 20 years of experience in their fields. As the independent representative of Emergo by UL in Turkiye, we offer a broad spectrum of compliance services, including regulatory strategy, medical device registration, quality management system compliance, and regulatory representation

CONTACT US

Any questions or remarks? Just write us a message!

E-MAIL

info@ardisglobal.com

CONTACT

ARDIS DANIŞMANLIK LTD. ŞTİ.
Company Headquarters: Göknar Sokak, Köse Apt. No:35/1 Muradiye, Beşiktaş, Istanbul, TURKEY
Branch Address: 5. Gazeteciler Sitesi Nilüfer Sokak, No:14 Akat Mahallesi, Beşiktaş, Istanbul, TURKEY

PHONE

(+90) 2122127347
(+90) 2125127347

ABOUT
Ardis Consulting delivers specialized consultancy services across the healthcare sector with a team that has over 20 years of experience in their fields.
SERVICES
Regulatory Compliance MDR&IVDR
Medical Device Registration
Registration Holder
Healthcare Market Research
CONTACT
Company Headquarters: Göknar Sokak, Köse Apt. No:35/1 Muradiye, Beşiktaş, Istanbul, TURKEY
Branch Address: 5. Gazeteciler Sitesi Nilüfer Sokak, No:14 Akat Mahallesi, Beşiktaş, Istanbul, TURKEY
(+90) 2122127347
info@ardisglobal.com