The recently introduced Medical Device Interim Regulations has made Saudi Arabia a regulated market for all types of medical devices. All manufacturers wishing to supply a Medical Device within Saudi Arabia now require Saudi Food & Drug Authority (SFDA) Market Authorisation. Manufacturers wishing to place goods in the Saudi market must now ...

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Ranked among the world's largest petrochemicals manufacturers, SABIC is a public company based in Riyadh, Saudi Arabia. 70% of the Company's shares are owned by the Saudi Arabian government, with the remaining 30% publicly traded on the Saudi stock exchange.

The most important users of desalinated water are in the Middle East, (mainly Saudi Arabia, Kuwait, the United Arab Emirates, Qatar and Bahrain), which uses about 70% of worldwide capacity; and in North Africa (mainly Libya and Algeria), which uses about 6% of worldwide capacity.

The SFDA guidance outlines the main requirements for the unique identification system to be applied for medical devices allowed to be imported and marketed in Saudi Arabia. According to the guidance, the medical device manufacturer shall be responsible for assigning the UDI to the device. The SFDA also emphasizes that the UDI marking is a ...

insurance in Saudi Arabia and the enforcement of the law are expected to translate into an increase in the number of beneficiaries and a wider utilisation of medical services at private healthcare facilities. • As of August 2019, there were 26 insurance companies operating in Saudi Arabia and the number of insured persons in the Kingdom stood

According to US press reports, Khashoggi family members in Saudi Arabia have already been given $10,000 a month and million-dollar houses by way of compensation.

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A royal decree of the Kingdom of Saudi Arabia (KSA) established a new medical device regulation, to take effect later this year. The Saudi Food and Drug Authority (SFDA) also extended the period during which GHTF registration applications would be accepted, published a guidance document on medical software utilizing artificial intelligence (AI) or big data, and updated the

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Under the Medical Devices Interim Regulation (MDIR), Decree No. 1-8-1429/2008, a medical device must have prior market authorization from one of these global health authorities (US, Japan, Australia, Canada or European Union), before being sold in the Kingdom of Saudi Arabia (KSA).

The Global Magnetoencephalography (MEG) Devices Market Research Report Forecast 2017-2021 is a valuable source of insightful data for business strategists. It provides the Magnetoencephalography (MEG) Devices industry overview with growth analysis and historical & futuristic cost, revenue, demand and supply data (as applicable).

In June, an EU anti-dumping investigation reached an interim finding (to be confirmed by December 2021) that Saudi Arabian MEG was exported to …

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Before selling in Saudi Arabia, device must be authorized in reference country (Australia, Canada, Europe, Japan, or USA) Appoint representative in Saudi Arabia. Representative must fill out an Authorized Representative (AR) contract, which will be reviewed by the SFDA. Submit Medical Device Marketing Authorization (MDMA) application through AR.

On 2 October 2018, Saudi government officials murdered Mr. Khashoggi in the Saudi consulate in Istanbul, Turkey. The Post quickly began its substantial coverage of the disappearance and murder investigation, expanding into reporting a number of related aspects of …

Market Overview: The Global Magnetoencephalography Devices Market held USD 276.1 million in 2019 and is to grow with a CAGR of 4.4% from 2020-2030. Magnetoencephalography Devices Market is growing at a much faster rate from the last few years. Magnetoencephalography problem occurs in all the age groups, but mostly to those who use more gadgets and do less exercises.

Medical Device Registration and Approval in Saudi Arabia General country-specific regulatory information is provided on this page for medical device registration and approval in Saudi Arabia. Become a LICENSALE.COM user to receive detailed device-specific compliance information for each market, including Saudi Arabia, to expedite the ...

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1.3. Conclusion. According to the Global Gender Gap Report, Saudi Arabia is one of worst countries globally in terms of human rights, freedom of opinion or equality.At the same time, Saudi Arabia is a country that already spends a lot of money on healthcare and will continue to increase this spending, making it an interesting market for medical device manufacturers.

Download this app from Microsoft Store for Windows 10, Windows 8.1, Windows 10 Mobile, Windows Phone 8.1. See screenshots, read the latest customer reviews, and compare ratings for MEG Audit Tool.

Shell's new 750,000 tonnes per annum MEG plant in Singapore is one of the world's largest, and the third facility worldwide, to use OMEGA technology. Other plants using OMEGA are operating in South Korea and Saudi Arabia. OMEGA delivers by far the lowest consumption of ethylene per tonne of MEG achieved so far in the industry. For every ...

In December 2019, India also started an anti-dumping probe into imports of MEG from Saudi Arabia, Kuwait, Oman, the UAE, and Singapore, Argaam said. Monoethylene glycol is used to make polyester ...

Medical Device Registration in Saudi Arabia. Click here to visit SFDA (Authority) website to learn more on medical device registration in Saudi Arabia. Labels to show the following: 1. The manufacturer name and address. 2. The EU representative details (name and address), for non-European manufacturer. 3.

Known as the 'pearl of Saudi Arabia', Ad Diriyah is set to put Saudi Arabia's tourism wheels in motion. It is the site of the first Saudi state, the original seat of power of Saudi Arabia's Al Saud family. Ad Diriyah is located on the outskirts of Riyadh, and is set to become a major tourist destination. The $17bn development will encompass ...

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The Saudi Food and Drug Authority (SFDA) have rolled out a single registration platform for all medical device market authorization called GHAD. According to updated guidance issued by SFDA and as per July 2021, local and foreign Medical Devices manufacturers are request to register or renew their licences under the new system GHAD. Here's what Swiss medtech exporters need to know about it.

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A consulting Firm in Saudi Arabia with SFDA - Medical Devices Registration with SFDA - Bio-Standards. Bio-Standards is a regulatory consultant specialized in product registration with the Saudi Food & Drug Authority (SFDA) for the following sectors: Medical devices, Human Medicine, Health and Herbal, Veterinary, Cosmetics, Food, Pesticide, and ...

How to use plugs from United States of America in Saudi Arabia . Plugs, sockets, adapters and other information needed for travelling from United States of America to Saudi Arabia in this page. If you want a report for other countries, re-start the wizard to find to electric adapters for your trip here. Quick Chart at …