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South Korea International Travel Information

If you spent time in South Korea during the past 14 days and feel sick with fever, cough, or difficulty breathing the Center for Disease Control and Prevention recommends individuals: Seek medical advice. Call ahead before going to a doctor’s office or emergency room. Tell them about your recent travel to South Korea, and your symptoms.

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ASTA Coronavirus Information & Resources | ASTA: The …

The FDA created a COVID-19 website that includes an FDA Q&A and additional information for food manufacturers. The Food Marketing Institute has additional information on the coronavirus, including information from the CDC that products and packages shipped to the U.S. from China pose a very low risk of spreading the virus.

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EU Strengthens Chemical Safety in Certain Toys | SGS

Nov 30, 2015 · The European Union (EU) has recently amended the Toy Safety Directive 2009/48/EC (TSD) to include the restriction of formamide and 4 preservatives in certain toys. The enforcement dates are dependent on the nature of the restricted substance and will start on 24 May 2017.

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Biocompatibility Evaluation of Breathing Gas Pathways | UL

Most medical device premarket reviews conducted by the FDA fall under its 510(k) Premarket Notification program. In addition to the device description, equivalent devices, software and performance testing information the FDA 510(k) submission must include data regarding the biocompatibility of any patient contacting materials, either directly ...

Gaming Reality - CNN

In South Korea, gaming can lead to fame and addiction. CNN follows one of the world's best "StarCraft II" players, who hopes to distance himself from gaming's dark side.

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U.S. Food and Drug Administration

The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the ...

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Exporters must be aware that Korea implements chemical residue maximum residue limits (MRLs) and microbiological requirements for meat products that may differ from Canadian requirements. Imported products are subject to testing on arrival in Korea and may be rejected when found out of compliance.

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Biocompatibility Evaluation of Breathing Gas Pathways | UL

The FDA is the federal agency responsible for the regulatory oversight of medical devices in the U.S. Most medical device premarket reviews conducted by the FDA …

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UL’s food and beverage testing, audit and inspection services help to protect brands and public health by managing and mitigating the challenges of today’s marketplace, from production to consumption.. UL puts safety at the top of the food chain. UL’s end to end Supply Chain Solution for the Food and Beverage industry include: Responsible Sourcing

COVID-19 IgG/IgM Rapid Test Cassette | Confirm BioSciences

COVID-19 IgG/IgM Rapid Test Cassette. The test, which is approved for sale in the EU and Internationally, is conducted by taking a small finger-prick blood sample, placing it in the center well of the cassette and then adding two drops of the buffer to the buffer well labeled “B.” Results should appear in 3 minutes and are invalid after 10 minutes.

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Establishment of the export certification program for FDA-regulated further processed eggs and egg product and composite foods containing egg products will allow U.S. processors access to expanding global markets supporting AMS goals in promoting the marketing of agricultural products.

EU Strengthens Chemical Safety in Certain Toys | SGS

The European Union (EU) has recently amended the Toy Safety Directive 2009/48/EC (TSD) to include the restriction of formamide and 4 preservatives in certain toys. The enforcement dates are dependent on the nature of the restricted substance and will start on 24 May 2017.

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4 days ago · At-home coronavirus tests: Everything you should know. Coronavirus testing shortages in the US are spurring private companies to develop at-home kits -- but the FDA is not on board (yet).

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FDA Approves Another New Weight Loss Drug - Forbes

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News & Perspective | CIDRAP

The declaration allows the president to exercise emergency powers and tap into $50 billion for relief efforts; Trump also announced a new public-private partnership to address the test shortage.

News & Perspective | CIDRAP

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