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New in Regulatory (page 4 of 26)
Jan 14, 2013 | 09:18 AM CST
They include (3-amino-3-carboxypropyl) dimethylsulfonium chloride, 2-ethyl-6-methylpyrazine, trimethylamine and trans-2-methyl-2-butenal.
Jan 14, 2013 | 08:07 AM CST
The organization has also opened up its scientific committee and panel meetings to external observers to promote better understanding of how scientific risk assessment is carried out.
Jan 08, 2013 | 11:54 AM CST
Notes the ingredient poses no toxicity concern for consumers at current levels of exposure and the current Acceptable Daily Intake (ADI) is safe for the general population.
Dec 19, 2012 | 11:34 AM CST
Panel finds 4-methylpent-3-en-2-one is not genotoxic; 4-methyl-3-hepten-5-one determination will be based on another group evaluation of a structurally equivalent substance.
Dec 05, 2012 | 11:53 AM CST
The results of Health Canada's evaluation of available data support the safety and efficacy of steviol glycosides when used as described.
Dec 05, 2012 | 10:40 AM CST
In response to two senators lobbying for stronger energy drink regulation, FDA says it's examining any casual risks to health, but notes other caffeine-containing products have a long history of safe use in the U.S.
Dec 03, 2012 | 12:55 PM CST
Effective Nov. 28, the rule establishes Jan. 1, 2016 as the uniform compliance date for food labeling regulations issued between Jan. 1, 2013, and Dec. 31, 2014
Nov 28, 2012 | 09:46 AM CST
In a final review, EFSA also says the Séralini et al study, "does not meet acceptable scientific standards," and there's "no need to re-examine previous safety evaluations."
Oct 15, 2012 | 08:18 AM CDT
Panel evaluated substances from flavoring group evaluation 304
Oct 09, 2012 | 10:49 AM CDT
S2383 and its four initial savory flavors were identified as flavoring substances that will be considered legal for use in EU countries as of the end of April 2013