Malaysian Health Authorities Grant Soy Protein Heart Claim

Malaysian Health Authorities Grant Soy Protein Heart Claim Malaysian authorities have ruled its nation's food manufacturers can claim foods containing soy protein help reduce a person's cholesterol.
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 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 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 Nutraceutical Clinical Laboratories International, Inc., Secures $2 Million in Funding KAVA ADVISORY: Health Canada is advising consumers not to use any products containing kava Garden of Life Settles Federal Trade Commission Complaint Garden of Life settles, admits no wrongdoing and has reveiwed all marketing and advertising material and worked cooperatively with FTC over past 18 months. Von Eschenbach nominated as FDA Commissioner President George W. Bush today announced his intention to nominate Andrew C. von Eschenbach, MD, to be Commissioner of the Food and Drug Administration. Von Eschenbach nominated as FDA Commissioner President George W. Bush today announced his intention to nominate Andrew C. von Eschenbach, MD, to be Commissioner of the Food and Drug Administration. Von Eschenbach nominated as FDA Commissioner President George W. Bush today announced his intention to nominate Andrew C. von Eschenbach, MD, to be Commissioner of the Food and Drug Administration. Von Eschenbach nominated as FDA Commissioner President George W. Bush today announced his intention to nominate Andrew C. von Eschenbach, MD, to be Commissioner of the Food and Drug Administration. Comment Period for Traditional Medicine Model Extended The draft document, “A Proposed Regulatory Model for Traditional Medicines: Guiding Assumptions and Key Components,” was released by the Traditional Medicines (TM) Congress, made up of nine national organizations, last November, with at least 70 comments received to date. Comment Period for Traditional Medicine Model Extended The draft document, “A Proposed Regulatory Model for Traditional Medicines: Guiding Assumptions and Key Components,” was released by the Traditional Medicines (TM) Congress, made up of nine national organizations, last November, with at least 70 comments received to date. 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. Statement by the National Nutritional Foods Association Regarding Today’s Introduction of Child Nutrition Promotion and School Lunch Protection Act in the Senate and House The National Nutritional Foods Association (NNFA) commends Sen. Tom Harkin (D-Iowa), Reps. Christopher Shays (R-Conn.) and Lynn Woolsey (D-Calif.), and co-sponsors, for introducing legislation addressing important issues pertaining to the health and nutrition of America’s children who rely on schools to provide nutritional and balanced foods as major components of a healthy, daily diet. Statement by the National Nutritional Foods Association Regarding Today’s Introduction of Child Nutrition Promotion and School Lunch Protection Act in the Senate and House The National Nutritional Foods Association (NNFA) commends Sen. Tom Harkin (D-Iowa), Reps. Christopher Shays (R-Conn.) and Lynn Woolsey (D-Calif.), and co-sponsors, for introducing legislation addressing important issues pertaining to the health and nutrition of America’s children who rely on schools to provide nutritional and balanced foods as major components of a healthy, daily diet. Natural Health Products Directorate Advises Not to Label Products as 'NPN Pending' Canada's Natural Health Products Directorate (NHPD) has issued a bulletin advising companies with products awaiting evaluation for product licenses not to label products these products with language describing the status as 'NPN Pending'. Natural Health Products Directorate Advises Not to Label Products as 'NPN Pending' Canada's Natural Health Products Directorate (NHPD) has issued a bulletin advising companies with products awaiting evaluation for product licenses not to label products these products with language describing the status as 'NPN Pending'. CRN 2006 Lobby Day This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ). CRN 2006 Lobby Day This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ). CRN 2006 Lobby Day This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ). CRN 2006 Lobby Day This year’s event included visits with 40 different House and Senate offices, including meetings with Sen. Orrin Hatch (R-UT), Sen. Dick Durbin (D-IL), Rep. Chris Cannon (R-UT), Rep. Mary Bono (R-CA) and Rep. Frank Pallone (D-NJ). NHPD Issues April Communiqué Health Canada's Natural Health Products Directorate (NHPD) has issued its April monthly Communiqué highlighting the announcement from earlier this week that the use of 'NPN Pending' on product labels is prohibited and noting other changes in risk categories and priority dates. NHPD Issues April Communiqué Health Canada's Natural Health Products Directorate (NHPD) has issued its April monthly Communiqué highlighting the announcement from earlier this week that the use of 'NPN Pending' on product labels is prohibited and noting other changes in risk categories and priority dates. Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated. Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated. Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated. Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated. Natural Health Products Directorate Places Food and Drink Format Product License Applications on Hold Canada's Natural Health Products Directorate, currently facing a backlog of over 10,000 product license applications, has placed all those products in a food or drink format on hold pending branch level review between the Natural Health Products Directorate and the Foods Directorate to determine under which category these products should be evaluated. Excellent Source Claim Allowed For Foods Containing Both EPA and DHA Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA). Excellent Source Claim Allowed For Foods Containing Both EPA and DHA Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA). Excellent Source Claim Allowed For Foods Containing Both EPA and DHA Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA). Excellent Source Claim Allowed For Foods Containing Both EPA and DHA Company announces the allowance of their petition for an Excellent Source Nutrient Content Claim for foods containing both EPA (Eicosapentaenoic Acid) and DHA (Docosahexaenoic Acid) under the authoritative statement provisions of the Food and Drug Modernization Act (FDAMA). CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S. Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI). CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S. Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI). CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S. Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI). CV Technologies Receives FDA Clearance to Sell COLD-fX'R' as a New Dietary Ingredient in U.S. Company announces that the unique patented active ingredient of the company's COLD-fX (CVT-E002) product has been accepted by the FDA as a New Dietary Ingredient (NDI). HHS/FDA on cGMPs: December 2006 The Department of Health and Human Services has forecast a date of December 2006 for the publication by the Food and Drug Administration of a final rule for current good manufacturing practice (cGMP) for dietary supplements. This projection was included in that department’s semiannual regulatory agenda of “potential rule-making” published in the Federal Register on April 24. HHS/FDA on cGMPs: December 2006 The Department of Health and Human Services has forecast a date of December 2006 for the publication by the Food and Drug Administration of a final rule for current good manufacturing practice (cGMP) for dietary supplements. This projection was included in that department’s semiannual regulatory agenda of “potential rule-making” published in the Federal Register on April 24. HHS/FDA on cGMPs: December 2006 The Department of Health and Human Services has forecast a date of December 2006 for the publication by the Food and Drug Administration of a final rule for current good manufacturing practice (cGMP) for dietary supplements. This projection was included in that department’s semiannual regulatory agenda of “potential rule-making” published in the Federal Register on April 24. Major Weight-Loss Marketers Pay $3 Million Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law, with the sttlements barring unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements. Major Weight-Loss Marketers Pay $3 Million Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law, with the sttlements barring unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements. Major Weight-Loss Marketers Pay $3 Million Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law, with the sttlements barring unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements. Major Weight-Loss Marketers Pay $3 Million Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law, with the sttlements barring unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements. Major Weight-Loss Marketers Pay $3 Million Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law, with the sttlements barring unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements. Major Weight-Loss Marketers Pay $3 Million Sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle Federal Trade Commission charges that their deceptive claims violated federal law, with the sttlements barring unsubstantiated claims in the future and bars the marketers from misrepresenting studies or endorsements. AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients. AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients. AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients. AHPA NDI Tele-Seminar Includes Essential Guidance Documents, NDI Database Subscription Discounts This week’s tele-seminar, Navigating FDA’s New Dietary Ingredient Notification Requirements, (May 19, 2006) will premiere the American Herbal Product Association's new Interim Guidance for New Dietary Ingredient Notifications for Manufacturers or Distributors of New Dietary Ingredients. CRN Responds To Panel Report On Multivitamins Organization responds to the report presented by the scientific panel at the NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention held this week in Bethesda, Md. CRN Responds To Panel Report On Multivitamins Organization responds to the report presented by the scientific panel at the NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention held this week in Bethesda, Md. 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. 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. 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. 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. 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. 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. 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. 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. Sageant Leads Grassroots Response to FTC Rule That Threatens Network Marketing Sageant has launched a national grassroots campaign to secure responses to the recently proposed Federal Trade Commission (FTC) new rule on business opportunities. Sageant Leads Grassroots Response to FTC Rule That Threatens Network Marketing Sageant has launched a national grassroots campaign to secure responses to the recently proposed Federal Trade Commission (FTC) new rule on business opportunities. NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle. NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle. NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle. NNFA Statement in Response to NIH State-of-the-Science Conference on Multivitamin/Mineral Supplements In response to findings by the State-of-the-Science Conference on Multivitamin/Mineral Supplements and Chronic Disease Prevention, the National Nutritional Foods Association (NNFA) maintains that multivitamins and other mineral supplements taken by more than 100 million Americans daily are a safe, affordable and effective way to maintain a healthy lifestyle. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. Peer-Reviewed Published Study Demonstrates Safety of UC-II® A recent study published in Toxicology Mechanisms and Methods demonstrates that UC-II®, InterHealth Nutraceuticals’ 40 mg, once-a-day, joint-health ingredient, is safe. BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate BioVittoria Announces the First Customer Beverage To Be Naturally Sweetened With Fruit-Sweetness™ Clorie-Free Fruit Concentrate Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. Jarrow Formulas® YouTube Channel Approaches 1 Million Views as Olympian-Endorsed Product Video Goes Viral The overwhelming popularity of the 26-second Olympian-endorsed product video, featuring short-track speed skater Katherine Reutter, reaps 1 million views for the Jarrow Formulas® YouTube Channel. ISO14001 certification granted to Indena Indena has been granted the ISO14001 certification for its main production site of Settala (Milan). ISO14001 certification granted to Indena Indena has been granted the ISO14001 certification for its main production site of Settala (Milan). ISO14001 certification granted to Indena Indena has been granted the ISO14001 certification for its main production site of Settala (Milan). ISO14001 certification granted to Indena Indena has been granted the ISO14001 certification for its main production site of Settala (Milan). ISO14001 certification granted to Indena Indena has been granted the ISO14001 certification for its main production site of Settala (Milan). New Company for “Change-The-World” Entrepreneurs™ Launches	ST. LOUIS, MO, May 04, 2006 (MARKET WIRE via COMTEX) -- Malaysian authorities have ruled its nation's food manufacturers can claim foods containing soy protein help reduce a person's cholesterol. The nutrient function claim decision was announced after The Solae Company, a leading researcher and manufacturer of soy protein food ingredients, petitioned Malaysian authorities to allow a heart health claim already approved in varying specificity by seven other nations. With the decision, food manufacturers in Malaysia may begin using the nutrient function claim on the labels of foods and beverages containing at least five grams of soy protein per serving, in conjunction with a statement explaining the amount required to reduce cholesterol in blood is 25 grams a day. "Malaysian authorities approved this claim after thoroughly examining 46 studies collected and submitted by our company," said Greg Paul, Ph.D., director of global health and nutrition at The Solae Company. "Their decision was made based upon an enormous and still growing body of data showing the heart health benefits of soy protein. It's the weight of this scientific evidence that has led so many other countries to authorize similar claims." High cholesterol is a leading risk factor for cardiovascular disease, which kills more than 16 million people worldwide each year and accounts for some 30 percent of all deaths. A number of studies have shown that consuming 25 grams of soy protein a day within a low fat, low cholesterol diet reduces a person's cholesterol level by approximately five percent, translating to a 10 percent reduction in a person's risk for developing heart disease. Researchers have found other ways in which soy protein may help reduce a person's risk for cardiovascular disease. Blood clots, for example, can completely block an artery already narrowed by atherosclerosis, a condition that causes a build up of waxy plaque inside blood vessels. Research findings suggest that certain properties found in soy foods may help prevent these blockages, reducing a person's chances of heart attack or stroke. Other studies have indicated soy protein may be linked with lower blood pressure. High blood pressure can lead to stroke, heart attack, heart failure and kidney failure. "Researchers continue to explore the positive benefits associated with soy protein, but more study is needed," said Dr. Paul. "As an industry leader, we will continue to invest in nutrition research that helps consumers make more informed decisions about what they eat." About The Solae Company The Solae Company is a food science and ingredient manufacturing organization, providing food and beverage manufacturers across the world with better ingredients for better living. Headquartered in St. Louis, Missouri, with regional offices in Brazil, Hong Kong and Switzerland, the company was formed through an alliance between Bunge Limited (BG) . For more information, visit www.solae.com.
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