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Georgia Medical Device Registration

Georgia Medical Device Regulation

Medical Device Regulation in Georgia: Market Overview, Registration Procedures, and Regulatory Compliance

Updated on 26/01/24

Regulatory Authority: State Regulation Agency for Medical Activities, Ministry of Labour, Health, and Social Affairs

Link for Ministry of Health:Ministry of Health (Georgia) | GHDx (healthdata.org)

Local Regulation:

Classification:

Listing or Registration Requirements:

Registration of medical devices in Georgia is not required, but prior to importation and marketing it would be necessary to obtain a letter from the Ministry of Labor, Health and Social Affairs of Georgia related to product classification.

 Documents Required for Registration:The registration process for dental materials, test systems, allergens, and reagents follow a similar procedure as that for medicinal products. According to the Law “On Medicinal Products,” registration can be conducted through either the national procedure, which takes 2 months, or the recognition procedure, with a registration period of 15 calendar days. The submission of documents aligns with an approved list.

Registration Timeline:

License Validity: The Marketing Authorization is granted for a duration of 5 years

Licence Renewal: In the case of a renewal procedure, applicable solely to products registered through the national procedure, documentation from the approved list must be submitted no later than 2 months before the expiration of the Marketing Authorization. The procedure typically spans 1 month, excluding the time allocated for responding to comments, which is 2 months.

Special Labelling Requirements:

Official documents, in English or Russian and bearing the original seal and signature from the manufacturer, are submitted for translation into Georgian, followed by notarization. Technical and clinical components are exclusively submitted in electronic format, available in English or Russian, with instructions from the manufacturer in the original, featuring a seal and signature, and provided in English, Russian, or both.

Who should make this communication:

  • Manufacturer

When to make this communication: Before placing a medical device into the market.

Market Overview:

The anticipated revenue for the Medical Devices market in Georgia is forecasted to reach US$134.20 million in 2024. Among the diverse market segments, US$21.25 million is expected to be the largest, contributing to a market volume of US$181.90 million in the same year. Looking forward, the industry is poised to undergo a consistent annual growth rate (CAGR 2024-2028) of 7.90%, leading to a projected market volume of US$181.90 million by 2028. It is noteworthy that, on a global scale, the United States is predicted to be the highest revenue generator, reaching US$182.00 billion in 2024. The medical devices market in Georgia is witnessing a surge in demand, particularly for advanced diagnostic equipment.

How OMC Medical can assist you with the process

  • Act as your Authorized representative

Why Choose Us

  • Working towards client satisfaction
  • Cost effective solutions
  • Project completion before deadline
  • Quality Regulatory affairs solutions

Contact us for free consultation: [email protected]

 

 

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