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14/05/2012 |
| Parliamentary Questions | |
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EU Parliamentary Question: Request for clarification on health claim evaluation
3 types of parliamentary questions are listed in Parliament's Rules of Procedure, in accordance with the Treaties and relevant interinstitutional ... |
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10/05/2012 |
| Other agencies opinion | |
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EFSA: ongoing discussions regarding health claims evaluations
The NDA Panel met last 25-27th of April 2012 in plenary sessions to discuss work in progress and adopt finalized scientific opinions. During the ... |
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07/05/2012 |
| Other agencies opinion | |
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United States: 2 ingredients achieved GRAS status
The Food and Drug Administration (FDA) has authorized the use of 2 ingredients in human food by awarding them GRAS status (Generally Recognized As ... |
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04/05/2012 |
| Other agencies opinion | |
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United States: 4 new GRAS applications under evaluation
The FDA (Food and Drug Administration) is studying GRAS (Generally Recognised As Safe) demands for 4 ingredients: - Cow's milk derived lactoferrin to ... |
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03/05/2012 |
| New regulatory texts | |
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The European Commission publishes implementing rules for Regulation (EC) No 1925/2006
Context: The Regulation No 1925/2006 of the European Parliament and of the Council of 20 December 2006 aims at ruling the addition of vitamins, ... |
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26/04/2012 |
| Other agencies opinion | |
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US: NAD requests further review on Serranol dietary supplement advertisement
Context: The National Advertising Division (NAD), an organisation responsible for evaluating the integrity of adverts in the United States, issued an ... |
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24/04/2012 |
| Other agencies opinion | |
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France: favorable opinion of ANSES for extending the use of a DHA-EPA-based Novel Food
Context: The French Agency for Food, Environmental and Occupational Health & Safety (ANSES) was asked by the DGCCRF (French Control Authority) on 20 ... |
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20/04/2012 |
| Other agencies opinion | |
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US: NAD approves conditionally ingredient-based claims for Urinozinc supplements
Context: The National Advertising Division (NAD), an organisation responsible for evaluating the integrity of adverts in the United States, recently ... |
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18/04/2012 |
| New regulatory texts | |
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New European regulation for food additives and colours
The new Commission Regulation (EU) No 231/2012 governing specifications for food additives including colours and sweeteners has been published in the ... |
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13/04/2012 |
| Other agencies opinion | |
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Novel Food: Unfavorable opinion for the substantial equivalence application between a Quinoa bran extract and Quinoa grain
Context: The French Agency for Food, environmental and occupational health safety (ANSES) has published its opinion related to a novel food ... |
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12/04/2012 |
| Other agencies opinion | |
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United States: 1 ingredient achieved GRAS status
Opinion: The Food and Drug Administration has recently authorized the use of CoroWiseTM phytosterols in human food by awarding them GRAS status ... |
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12/04/2012 |
| Other agencies opinion | |
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United States: 3 new ingredients under evaluation
The FDA (Food and Drug Administration) is studying GRAS (Generally Recognised As Safe) demands for three ingredients: - Sucrose fatty acid esters ... |
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11/04/2012 |
| Other agencies opinion | |
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Novel food: favorable ANSES opinion on synthetic vitamin K2
Context: The French Agency for Food, Environmental and Occupational Health Safety (ANSES) has been requested by the DGCCRF (French Control Authority) ... |
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10/04/2012 |
| Regulatory proposals in EU | |
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New European Directive prohibits added sugars in fruit juices
Context: Following a first-reading agreement with the European Parliament, the European Council approved on 8 March 2012 the revision of the Directive ... |
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06/04/2012 |
| EFSA opinion | |
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EFSA releases final guidance on appetite ratings, weight management, and blood glucose concentrations
The European Food Safety Authority (EFSA) recently published final guidance on scientific requirements for health claims related to appetite ratings, ... |
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