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Once-a-Day Pill for Hepatitis C Wins Fda Ok
2014-10-11 00:00:51| Biotech - Topix.net
Federal health officials have approved a daily pill that can cure the most common form of hepatitis C without the grueling pill-and-injection cocktail long used to treat the virus. But the drug's $1,125-per-pill price is sure to increase criticism of drugmaker Gilead Sciences, whose pricing strategy for an older hepatitis drug has already drawn scorn from patient groups, insurers and politicians worldwide.
FDA Amends Four Core FSMA Rules
2014-10-10 16:52:00| Food Processing
Changes to human foods, animal foods, produce safety and foreign supplier verification program.
Sodium acid pyrophosphate (SAPP) doesn't belong in foods labeled 'all-natural', FDA warns baker
2014-10-06 21:02:00| Grocery - Topix.net
FDA: 'Your products are misbranded because they bear the claim 'All Natural' but contain sodium acid pyrophosphate, which is a synthetic substance' Leavening agent sodium acid pyrophosphate doesn't belong in products making 'all-natural' claims, even if they are USDA certified organic, the FDA has told a Massachusetts-based baker. " Your liveGfree Blueberry Pancakes are misbranded within the meaning of Section 403 of the Act [21 U.S.C. A 343 ] because [they] bear the claim 'All Natural' but contain sodium acid pyrophosphate, which is a synthetic substance."
Sodium acid pyrophosphate (SAPP) doesn't belong in foods labeled 'all-natural', FDA warns baker
2014-10-06 17:15:20| Food - Topix.net
FDA: 'Your products are misbranded because they bear the claim 'All Natural' but contain sodium acid pyrophosphate, which is a synthetic substance' Leavening agent sodium acid pyrophosphate doesn't belong in products making 'all-natural' claims, even if they are USDA certified organic, the FDA has told a Massachusetts-based baker. " Your liveGfree Blueberry Pancakes are misbranded within the meaning of Section 403 of the Act [21 U.S.C. A 343 ] because [they] bear the claim 'All Natural' but contain sodium acid pyrophosphate, which is a synthetic substance."
FDA Aims to Shore Up Medical Device Cybersecurity
2014-10-06 16:00:00| TechNewsWorld
The Food and Drug Administration last week released long-awaited recommendations aimed at better managing cybersecurity risks to protect patient health and information. The new standards recommend manufacturers take into account cybersecurity risks as part of the design and development of a medical device. They require device makers to submit documentation to the FDA about identified risks.
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