European Parliament Passes Second Reading On Fortified Foods Regulations

European Parliament Passes Second Reading On Fortified Foods Regulations The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
Home Naturade Significantly Strengthens Balance Sheet; Receives $2.5 Million in Capital from Westgate Equity Partners, L.P. Natrol Appoints Vincent Andrich VP Sales for Prolab Division Vermont Pure Holdings, Ltd. Announces Record Fiscal Year 2001 Results Body Shop Reports 24.8 Mil Euro Sales Revenues Spectrum Organic Products Responds to FDA Letter Regarding Use of Non-GMO Seal on Canola Oil Label Supplement Group Targets Consumer Education Advanced Nutraceuticals, Inc. Announces 2001 Year End Results And Additional Financing ADM Awarded Nutraceuticals Patent Patent Creates Proprietary Position for ADM in Fast-Growing Nutraceutical Market Tantivy Sciences Obtains Exclusive License to Unique Nutraceutical Products Top GNC Executives Tour Pittsburgh Market to Present New Business Plan and Expansion Possibilities; Meeting will focus on new business strategies and growth Nutrition 21 Receives Patent For the Nutritional Treatment of Type 2 Diabetes; Patent Presents New Pharmaceutical Licensing Opportunities ConsumerLab.com Finds Most B-vitamin Supplements Contain What They Claim, But Often Exceed Safe Levels - Consumers Cautioned to Be Aware of Side Effects with High Dose Products Nutraceutix, Inc., Nutravite Announcement Commercial Availability of CDT™ Glucosamine for Canadian Marketplace Harvey Kamil Appointed President of NBTY, Inc. - Scott Rudolph to Continue as Chairman and CEO drugstore.com Expects to Reach Profitability Target in 2003 Human Genome Project Leads to Innovative Healthcare NPIcenter’s Career Center targets nutraceutical Industry Adding Vitamin C To Certain Drugs May Help Treat Alzheimer's, Other Brain Disorders Adding Vitamin C To Certain Drugs May Help Treat Alzheimer's, Other Brain Disorders Editorial: An Exercise in Synergy NBTY, Inc. Appoints Harvey Kamil President, Scott Rudolph To Continue As Chairman And CEO Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids LignisulMSM vs Naproxen for Osteoarthritis Clinical Trial Gets Underway Natural Health Trends Corp. Launches Lexxus Taiwan FDA Presents Compliance Guide for Structure/Function Claims New TrimFit® Bars Redefine Energy Bar Category New TrimFit® Bars Redefine Energy Bar Category Probiata® Offers Safe, Natural and Effective Alternative Alive & Well with Michelle Harris Be Well and Get Rewarded! Find Personalized Wellness Solutions and Earn Free Vitamins at NatureMade.com Consumers Search for Healthy Cleaning Products That Work Nordic Naturals: Omega 3 Fatty Acids Cyanotech Names Bob Capelli as Director of Sales Report on the Codex Nutrition Committee Meeting in Bonn, Germany Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting. Report on the Codex Nutrition Committee Meeting in Bonn, Germany Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting. Report on the Codex Nutrition Committee Meeting in Bonn, Germany Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting. Report on the Codex Nutrition Committee Meeting in Bonn, Germany Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting. Report on the Codex Nutrition Committee Meeting in Bonn, Germany Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting. FSA Receives Plant sterols application DDO Processing has asked that their phytosterols extract from tall oil be regarded as equivalent to a previously approved tall oil extract. FSA Receives Plant sterols application DDO Processing has asked that their phytosterols extract from tall oil be regarded as equivalent to a previously approved tall oil extract. FSA Receives Plant sterols application DDO Processing has asked that their phytosterols extract from tall oil be regarded as equivalent to a previously approved tall oil extract. FSA Receives Plant sterols application DDO Processing has asked that their phytosterols extract from tall oil be regarded as equivalent to a previously approved tall oil extract. FSA Receives Plant sterols application DDO Processing has asked that their phytosterols extract from tall oil be regarded as equivalent to a previously approved tall oil extract. Navamedic Obtains Glucosamine HCl Product Approval in 19 European Countries Navamedic's glucosamine HCl product has been approved in 19 countries for treatment of osteoarthritis of the knee. The product was approved in Sweden in August 2005, and has now been reviewed in the European Mutual Recognition Procedure. Navamedic Obtains Glucosamine HCl Product Approval in 19 European Countries Navamedic's glucosamine HCl product has been approved in 19 countries for treatment of osteoarthritis of the knee. The product was approved in Sweden in August 2005, and has now been reviewed in the European Mutual Recognition Procedure. Navamedic Obtains Glucosamine HCl Product Approval in 19 European Countries Navamedic's glucosamine HCl product has been approved in 19 countries for treatment of osteoarthritis of the knee. The product was approved in Sweden in August 2005, and has now been reviewed in the European Mutual Recognition Procedure. Navamedic Obtains Glucosamine HCl Product Approval in 19 European Countries Navamedic's glucosamine HCl product has been approved in 19 countries for treatment of osteoarthritis of the knee. The product was approved in Sweden in August 2005, and has now been reviewed in the European Mutual Recognition Procedure. Navamedic Obtains Glucosamine HCl Product Approval in 19 European Countries Navamedic's glucosamine HCl product has been approved in 19 countries for treatment of osteoarthritis of the knee. The product was approved in Sweden in August 2005, and has now been reviewed in the European Mutual Recognition Procedure. Navamedic Obtains Glucosamine HCl Product Approval in 19 European Countries Navamedic's glucosamine HCl product has been approved in 19 countries for treatment of osteoarthritis of the knee. The product was approved in Sweden in August 2005, and has now been reviewed in the European Mutual Recognition Procedure. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. Cantox and Others Host US and EU Legal and Claims Comparative Analysis Workshop CANTOX, along with Law firms (Coutrelis & Associes and Hyman, Phelps & McNamara, PC) will be hosting a workshop on Tuesday, April 4, 2006 in Washington, DC, to provide a comparative analysis of the current US and EU legal frameworks and scientific health claim substantiation standards. UK Food Standards Agency board Discusses Folate and Health Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification. UK Food Standards Agency board Discusses Folate and Health Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification. UK Food Standards Agency board Discusses Folate and Health Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification. UK Food Standards Agency board Discusses Folate and Health Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification. UK Food Standards Agency board Discusses Folate and Health Food Standards Agency (FSA) Board today agreed to consult on options for improving the folate status of young women; options include voluntary or mandatory fortification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. European Parliament Passes Second Reading on Health and Nutrition Claims The European Parliament has passed second reading of the Health and Nutrition Claims Regulation which will govern permitted health and nutrition claims allowable in the European Union. The regulations, incorporating compromise amendments introduced prior to this reading, are expected to be formally adopted by this autumn. The regulation includes strict conditions for nutrition claims, an initial positive list of approved health claims (after which claims submitted will have to be reviewed by the European Food Safety Authority (EFSA) and then approved by the Commission and Member States), and the use of new health claims or disease reduction claims will require specific authorization after scientific assessment and verification. UK's MHRA to Require Label Warning on Black Cohosh The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.” UK's MHRA to Require Label Warning on Black Cohosh The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.” UK's MHRA to Require Label Warning on Black Cohosh The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.” UK's MHRA to Require Label Warning on Black Cohosh The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.” UK's MHRA to Require Label Warning on Black Cohosh The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.” UK's MHRA to Require Label Warning on Black Cohosh The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.” Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries. EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels UK: Views Sought on Noni Juice Opinion The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product. UK: Views Sought on Noni Juice Opinion The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product. UK: Views Sought on Noni Juice Opinion The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product. UK: Views Sought on Noni Juice Opinion The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product. UK: Views Sought on Noni Juice Opinion The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. Baywood's Cal-Mag FIZZ Product Approved by European Union Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries. UK: Comments needed on phytosterol application Lipofoods, has asked the UK Food Standards Agency's expert advisers on novel foods for an opinion on the ‘equivalence’ of a phytosterol ingredient to be used in various foods. UK: Comments needed on phytosterol application Lipofoods, has asked the UK Food Standards Agency's expert advisers on novel foods for an opinion on the ‘equivalence’ of a phytosterol ingredient to be used in various foods. Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award The 2009 Frost & Sullivan European Functional Food & Beverage Microencapsulation Technology Innovation Award has been presented to GAT Food Essentials GmbH in recognition of its proprietary wowCAPS(R) technology. Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award The 2009 Frost & Sullivan European Functional Food & Beverage Microencapsulation Technology Innovation Award has been presented to GAT Food Essentials GmbH in recognition of its proprietary wowCAPS(R) technology. Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award The 2009 Frost & Sullivan European Functional Food & Beverage Microencapsulation Technology Innovation Award has been presented to GAT Food Essentials GmbH in recognition of its proprietary wowCAPS(R) technology. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates Bio-Extraction Inc., has announced that it has completed the self-affirmation process to qualify its specialty canola protein products, Isolexx(TM) and Vitalexx(TM), as self-affirmed GRAS for their intended use in various foods and beverages, thus providing a basis for the sale of these products in the United States when commercial production commences in Q1 2010. Synergy Flavors Invests in Sensory Flavor Profiling Research Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients. Synergy Flavors Invests in Sensory Flavor Profiling Research Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients. Synergy Flavors Invests in Sensory Flavor Profiling Research Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients. Synergy Flavors Invests in Sensory Flavor Profiling Research Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients. Synergy Flavors Invests in Sensory Flavor Profiling Research Synergy Flavors has commissioned a new research program at North Carolina State University to study the sensory profiles of a range of protein ingredients. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Synergy Flavors Inc., has announced their chocolate flavors offer a versatile solution for cocoa reduction and can be used as cocoa extenders. NPI Daily - Top of The News for Nov. 20, 2009 - FDA Issues 22 Warning Letters to Website Operators Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award; Synergy Flavors Invests in Sensory Flavor Profiling Research; FDA Issues 22 Warning Letters to Website Operators; Nordic Naturals Ultimate Omega™ First Fish Oil to Participate in NFL/NFLPA Sports Nutrition Label Certification Program; BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates; New Organic Berry Whole Food Energy Bar from Amazing Grass Delivers Whole Food Nutrition; Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors NPI Daily - Top of The News for Nov. 20, 2009 - FDA Issues 22 Warning Letters to Website Operators Frost & Sullivan Honours GAT Food Essentials GmbH With European Functional Food & Beverage Microencapsulation Technology Innovation Award; Synergy Flavors Invests in Sensory Flavor Profiling Research; FDA Issues 22 Warning Letters to Website Operators; Nordic Naturals Ultimate Omega™ First Fish Oil to Participate in NFL/NFLPA Sports Nutrition Label Certification Program; BioExx Achieves Self-Affirmed GRAS Status for Protein Isolates; New Organic Berry Whole Food Energy Bar from Amazing Grass Delivers Whole Food Nutrition; Beat Crazy Cocoa Prices with Synergy's Chocolate Flavors Heart Health Alert: Niacin May Reverse Hardening of the Arteries Heart Health Alert: Niacin May Reverse Hardening of the Arteries Heart Health Alert: Niacin May Reverse Hardening of the Arteries Heart Health Alert: Niacin May Reverse Hardening of the Arteries Spotlight on Savory Side Dishes Spotlight on Savory Side Dishes Spotlight on Savory Side Dishes Another Reason to Choose Healthy Lifestyle Habits Another Reason to Choose Healthy Lifestyle Habits	Earlier this week, the European Parliament held its second reading vote on proposed Fortified Foods Regulations, intended to put in place common EU rules on the addition of vitamins, minerals and other substances to foods. A positive list of vitamins and minerals that can be added to food is included in the proposed Regulation, as are criteria for setting minimum and maximum levels for such nutrients in food. There is a transitional period of 7 years in which vitamins and minerals not on the EU list may remain on the market, provided that they were added to foods marketed in the EU at the time the Regulation entered into force and that dossiers supporting their use are submitted to the Commission within 3 years of the Regulation entering into force. These dossiers will then be transferred to the European Food Safety Authority (EFSA) for evaluation. The Regulation also sets out a procedure to scrutinize and, if necessary, restrict or forbid the use of substances other than vitamins and minerals whose addition to foodstuffs would lead to an excessive intake of the substance. The European Council is expected to formally adopt the Regulation in the coming weeks, and it will enter into force 20 days after its publication in the Official Journal of the European Communities. The new rules on fortification will start to apply 6 months from this date, although for up to 3 years afterwards, products not in compliance with the Regulation will still be allowed to be marketed, provided that they were labeled or placed on the market prior its entry into force. Minimum and maximum levels for the addition of different nutrients to food will be established through the Comitology procedure based on scientific advice from EFSA. The Commission intends to publish a discussion paper on these levels within the coming months, and within 2 years of the adoption of the Regulation, it plans to put forward proposed levels for agreement by Member States in the Standing Committee on the Food Chain.
Powered By Traffic Booster Absolute News Manager Plug-in by Xigla Software