Overview on Medical Device Registration in Qatar
Update On: 24/01/2024
Regulatory Authority: Ministry of Public Health
Link for Regulatory Authority: https://www.moph.gov.qa/english/Pages/default.aspx
Local Regulation:
Classification: Class I, IIa, IIb, III and IV
Listing or Registration Requirements:No registration required.
Documents Required:
Registration Timeline:
Registration Fee:
License Validity:
Special Labelling Requirements:
Additional Comments:Medical devices must be authorized by one of the founding members of the Global Harmonization Task Force (GHTF) to obtain market access. A local authorized representative is required to obtain an import permit.
Who should make this communication:
When to make this communication: Before placing a medical device into the market.
How OMC Medical can assist you with the process
Why Choose Us
Contact us for free consultation: [email protected]
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
To launch a medical device in a country, medical devices must comply with the local country’s regulatory requirements. Let us be your trusted partner in bringing your medical devices to the Global market. Contact us today to learn more about how we can assist you in every step of the way.