Report on the Codex Nutrition Committee Meeting in Bonn, Germany

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.
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 Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Food Supplements Directive: European Court of Justice Rules in Favour of the Commission The European Court of Justice (ECJ) ruled in favour of the European Commission, upholding the validity of the Food Supplements Directive, its legal base and the positive list system. Five Hundred Dossiers Submitted to Agency on Safety of Food Supplements Agency has received 500 dossiers from the supplements industry providing information on vitamins and minerals to enable the European Food Safety Authority (EFSA) to make safety assessments. Five Hundred Dossiers Submitted to Agency on Safety of Food Supplements Agency has received 500 dossiers from the supplements industry providing information on vitamins and minerals to enable the European Food Safety Authority (EFSA) to make safety assessments. Five Hundred Dossiers Submitted to Agency on Safety of Food Supplements Agency has received 500 dossiers from the supplements industry providing information on vitamins and minerals to enable the European Food Safety Authority (EFSA) to make safety assessments. Five Hundred Dossiers Submitted to Agency on Safety of Food Supplements Agency has received 500 dossiers from the supplements industry providing information on vitamins and minerals to enable the European Food Safety Authority (EFSA) to make safety assessments. Five Hundred Dossiers Submitted to Agency on Safety of Food Supplements Agency has received 500 dossiers from the supplements industry providing information on vitamins and minerals to enable the European Food Safety Authority (EFSA) to make safety assessments. Five Hundred Dossiers Submitted to Agency on Safety of Food Supplements Agency has received 500 dossiers from the supplements industry providing information on vitamins and minerals to enable the European Food Safety Authority (EFSA) to make safety assessments. Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Metafolin ruled safe for use in supplements and foods by JECFA Company announces that Metafolin, its new patented form of folate, has been approved as a safe alternative to folic acid for use in dietary supplements, foods for special dietary uses and other foods by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. What Next For Food Supplements In Europe? Conference: Food Supplements in Europe, Challenges for the Future Government representatives from the food and health sectors of more than twenty EU and non-EU countries met with the European Commission, scientific experts and the food supplement industry in Berlin in September to debate the next stages of development of the regulatory environment for Food Supplements; delegates explored common approaches on the setting of maximum levels for vitamins and minerals, the substantiation of health claims , and potential models for the safety assessment of ingredients other than vitamins and minerals. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. Final Dietary Supplement cGMP at OMB; AHPA to Offer Training through Teleseminars The Office of Management and Budget (OMB) has recorded that it has received the final good manufacturing practice (cGMP) rule for dietary supplements for review. 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. Metafolin Approved for Use in Dietary Supplements and Dietetic Foods in EU The Metafolin® form of folate, will soon be added to the positive list of vitamins for food supplements and foods for particular nutritional uses by the EU Standing Committee on the Food Chain and Animal Health (SCFCAH). Metafolin Approved for Use in Dietary Supplements and Dietetic Foods in EU The Metafolin® form of folate, will soon be added to the positive list of vitamins for food supplements and foods for particular nutritional uses by the EU Standing Committee on the Food Chain and Animal Health (SCFCAH). Metafolin Approved for Use in Dietary Supplements and Dietetic Foods in EU The Metafolin® form of folate, will soon be added to the positive list of vitamins for food supplements and foods for particular nutritional uses by the EU Standing Committee on the Food Chain and Animal Health (SCFCAH). Metafolin Approved for Use in Dietary Supplements and Dietetic Foods in EU The Metafolin® form of folate, will soon be added to the positive list of vitamins for food supplements and foods for particular nutritional uses by the EU Standing Committee on the Food Chain and Animal Health (SCFCAH). 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. 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.” 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. Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink Nestle has announced the release of their BOOST(R) Kid Essentials Nutritionally Complete Drink. The drink is designed to give probiotics, delivered through the BOOST Kid Essentials straw, and contains 25 essential vitamins and minerals, seven grams of protein, antioxidants and 244 calories. Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink Nestle has announced the release of their BOOST(R) Kid Essentials Nutritionally Complete Drink. The drink is designed to give probiotics, delivered through the BOOST Kid Essentials straw, and contains 25 essential vitamins and minerals, seven grams of protein, antioxidants and 244 calories. Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink Nestle has announced the release of their BOOST(R) Kid Essentials Nutritionally Complete Drink. The drink is designed to give probiotics, delivered through the BOOST Kid Essentials straw, and contains 25 essential vitamins and minerals, seven grams of protein, antioxidants and 244 calories. Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink Nestle has announced the release of their BOOST(R) Kid Essentials Nutritionally Complete Drink. The drink is designed to give probiotics, delivered through the BOOST Kid Essentials straw, and contains 25 essential vitamins and minerals, seven grams of protein, antioxidants and 244 calories. Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink Nestle has announced the release of their BOOST(R) Kid Essentials Nutritionally Complete Drink. The drink is designed to give probiotics, delivered through the BOOST Kid Essentials straw, and contains 25 essential vitamins and minerals, seven grams of protein, antioxidants and 244 calories. Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink Nestle has announced the release of their BOOST(R) Kid Essentials Nutritionally Complete Drink. The drink is designed to give probiotics, delivered through the BOOST Kid Essentials straw, and contains 25 essential vitamins and minerals, seven grams of protein, antioxidants and 244 calories. Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." Health Canada Releases January 2009 Issue of CARN Health Canada has released their January 2009 issue of the Canadian Adverse Reaction Newsletter, which works to help alert "health professionals to potential signals detected through the review of case reports submitted to Health Canada." NPI Daily - Top of The News for January 8, 2009 - HHS Officials Mark Opening of First U.S. Food and Drug Administration Office in Latin America Natural Alternatives International, Inc. Announces Change in Executive Officer and Loan Modification and Extension; BBB Warns Consumers of Two Companies That Use Oprah, Other Celebrity Names, to Sell Supplements; HHS Officials Mark Opening of First U.S. Food and Drug Administration Office in Latin America; dicentra Web Seminar on Challenges and Solutions for Registering a Probiotic Product with the NHPD; Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink; Health Canada Releases January 2009 Issue of CARN; What to Expect From the Nutrition Industry's Ingredient Supply Segment in 2009 NPI Daily - Top of The News for January 8, 2009 - HHS Officials Mark Opening of First U.S. Food and Drug Administration Office in Latin America Natural Alternatives International, Inc. Announces Change in Executive Officer and Loan Modification and Extension; BBB Warns Consumers of Two Companies That Use Oprah, Other Celebrity Names, to Sell Supplements; HHS Officials Mark Opening of First U.S. Food and Drug Administration Office in Latin America; dicentra Web Seminar on Challenges and Solutions for Registering a Probiotic Product with the NHPD; Nestle Nutrition Launches BOOST® Kid Essentials Nutritionally Complete Drink; Health Canada Releases January 2009 Issue of CARN; What to Expect From the Nutrition Industry's Ingredient Supply Segment in 2009 Something To Feel Good About: New Study Validates St. John's Wort Efficacy in Support against Depression Bioforce USA has announced the results of a clinical survey of 200 patients suffering from mild to moderate depression and the effects of six weeks of taking St. Johns Wort (A. Vogel Hyperiforce) tablets. The year-long study (March 2006 to March 2007) recruited 33 physicians in private practices in Switzerland. The study looked at several factors of the state of depression itself: severity, anxiety and nervousness, as well as vegetative (physical/systemic) symptoms. Something To Feel Good About: New Study Validates St. John's Wort Efficacy in Support against Depression Bioforce USA has announced the results of a clinical survey of 200 patients suffering from mild to moderate depression and the effects of six weeks of taking St. Johns Wort (A. Vogel Hyperiforce) tablets. The year-long study (March 2006 to March 2007) recruited 33 physicians in private practices in Switzerland. The study looked at several factors of the state of depression itself: severity, anxiety and nervousness, as well as vegetative (physical/systemic) symptoms. Something To Feel Good About: New Study Validates St. John's Wort Efficacy in Support against Depression Bioforce USA has announced the results of a clinical survey of 200 patients suffering from mild to moderate depression and the effects of six weeks of taking St. Johns Wort (A. Vogel Hyperiforce) tablets. The year-long study (March 2006 to March 2007) recruited 33 physicians in private practices in Switzerland. The study looked at several factors of the state of depression itself: severity, anxiety and nervousness, as well as vegetative (physical/systemic) symptoms. Something To Feel Good About: New Study Validates St. John's Wort Efficacy in Support against Depression Bioforce USA has announced the results of a clinical survey of 200 patients suffering from mild to moderate depression and the effects of six weeks of taking St. Johns Wort (A. Vogel Hyperiforce) tablets. The year-long study (March 2006 to March 2007) recruited 33 physicians in private practices in Switzerland. The study looked at several factors of the state of depression itself: severity, anxiety and nervousness, as well as vegetative (physical/systemic) symptoms. Something To Feel Good About: New Study Validates St. John's Wort Efficacy in Support against Depression Bioforce USA has announced the results of a clinical survey of 200 patients suffering from mild to moderate depression and the effects of six weeks of taking St. Johns Wort (A. Vogel Hyperiforce) tablets. The year-long study (March 2006 to March 2007) recruited 33 physicians in private practices in Switzerland. The study looked at several factors of the state of depression itself: severity, anxiety and nervousness, as well as vegetative (physical/systemic) symptoms. Something To Feel Good About: New Study Validates St. John's Wort Efficacy in Support against Depression Bioforce USA has announced the results of a clinical survey of 200 patients suffering from mild to moderate depression and the effects of six weeks of taking St. Johns Wort (A. Vogel Hyperiforce) tablets. The year-long study (March 2006 to March 2007) recruited 33 physicians in private practices in Switzerland. The study looked at several factors of the state of depression itself: severity, anxiety and nervousness, as well as vegetative (physical/systemic) symptoms. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Proprietary Nutritionals to Distribute Sytrinol Heart Health Supplement Dean Mosca, president of Proprietary Nutritionals, Inc., has announced that PNI will assume the exclusive worldwide distribution rights for Sytrinol®, effective Jan. 1, 2009. Natural Products Association Advocates Strength of Dietary Supplement Law The Natural Products Association's Executive Director and CEO, David Seckman, has released a statement in response to misleading statements recently made regarding dietary supplement regulation. Natural Products Association Advocates Strength of Dietary Supplement Law The Natural Products Association's Executive Director and CEO, David Seckman, has released a statement in response to misleading statements recently made regarding dietary supplement regulation. Natural Products Association Advocates Strength of Dietary Supplement Law The Natural Products Association's Executive Director and CEO, David Seckman, has released a statement in response to misleading statements recently made regarding dietary supplement regulation. Natural Products Association Advocates Strength of Dietary Supplement Law The Natural Products Association's Executive Director and CEO, David Seckman, has released a statement in response to misleading statements recently made regarding dietary supplement regulation. Natural Products Association Advocates Strength of Dietary Supplement Law The Natural Products Association's Executive Director and CEO, David Seckman, has released a statement in response to misleading statements recently made regarding dietary supplement regulation. Natural Products Association Advocates Strength of Dietary Supplement Law The Natural Products Association's Executive Director and CEO, David Seckman, has released a statement in response to misleading statements recently made regarding dietary supplement regulation.	The Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) met last week in Bonn with over 300 delegates from 70 countries participating. Participants report little progress on key issues for the food supplements industry, as further consideration of these issues will await decisive discussions at the committee's next meeting next year in Thailand. Some specifics of the Bonn discussions include: DRAFT PROPOSED RECOMMENDATIONS ON THE SCIENTIFIC BASIS OF HEALTH CLAIMS: France, the country with the mandate to draft these draft recommendations, highlighted a number of questions for consideration to build the text better, and the committee decided that the Codex Secretariat would send out a Circular Letter to all member countries and observers requesting comments on the questions, and on how to proceed with this work. France would then revise the draft based on these comments. APPLICATION OF RISK ANALYSIS TO THE WORK OF THE CCNFSDU: The Working Group led by Australia is requested to give further consideration on this issue with the aim of presenting a proposal for new work on Risk Analysis at the next meeting of the Committee, with the intention to submit it, if agreed by the Committee, at the meeting of the Codex Alimentarius Commission in 2007.
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