The medical device importer in Qatar has several key responsibilities to ensure compliance with regulatory requirements:
1. They must appoint a local authorized representative to handle regulatory matters.
2. Obtain an import permit from the Ministry of Public Health through the representative.
3. Provide necessary documentation including a Certificate of Free Sale, import license, and company/product registration.
4. Ensure registration of implantable devices with the Ministry of Public Health.
5. Verify the manufacturer’s quality management system and certification.
6. Confirm implementation of a risk management system by the manufacturer.
7. Ensure proper labeling and packaging of medical devices.
8. Guarantee compliance with Qatari regulations regarding safety, efficacy, and quality.
9. Ensure the manufacturer has a post-market surveillance system.
10. Maintain continuous compliance throughout the product’s lifecycle.
Contact us for free consultation: info@omcmedical.co.uk
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.
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