FDA Commissioner Lester Crawford Resigns

FDA Commissioner Lester Crawford Resigns US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately.
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 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). Food & Drug Administration approves LycoMato® as safe color additive FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries. Food & Drug Administration approves LycoMato® as safe color additive FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries. Food & Drug Administration approves LycoMato® as safe color additive FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries. Food & Drug Administration approves LycoMato® as safe color additive FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries. Food & Drug Administration approves LycoMato® as safe color additive FDA is amending its color additive regulations to provide for the safe use of LycoMato® tomato lycopene extract as a color additive in foods, in response to a Color Additive Petition filed by LycoRed Natural Products Industries. Effective Date of AHPA Trade Recommendations Nears Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels. Effective Date of AHPA Trade Recommendations Nears Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels. Effective Date of AHPA Trade Recommendations Nears Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels. Effective Date of AHPA Trade Recommendations Nears Recommendations include: appropriate steps be taken to assure that black cohosh rhizome and root raw material is free of its known adulterant, Chinese cimicifuga rhizome and root, and dislosure of caffeine on product labels. AHPA Tele-Seminar to Help Companies Understand How FDA Inspections Should be Conducted and Managed Tele-seminars are scheduled to begin at 2 pm ET / 11 am PT on August 30 and September 8, 2005; each seminar will be limited to just 30 call lines. AHPA Tele-Seminar to Help Companies Understand How FDA Inspections Should be Conducted and Managed Tele-seminars are scheduled to begin at 2 pm ET / 11 am PT on August 30 and September 8, 2005; each seminar will be limited to just 30 call lines. FDA Review Period Extended for Nutrition 21's Chromium Picolinate Diabetes-Related Qualified Health Claim Petition Company agrees to fDA's request to extend review period for two weeks. FDA Review Period Extended for Nutrition 21's Chromium Picolinate Diabetes-Related Qualified Health Claim Petition Company agrees to fDA's request to extend review period for two weeks. FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.” FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.” FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.” FDA Approves First Qualified Health Claim for Chromium Picolinate and Risk of Type 2 Diabetes FDA has concluded that there is credible evidence to support the following qualified health claim: “One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain.” FDA Publishes Guidance for Bioterrorism Recordkeeping Requirements FDA announced the publication of a guidance document on the recordkeeping requirements of the Bioterrorism Act; the guidance topics include who must comply with and who is excluded from the rule, and what information is required to be kept and made available to FDA during a Bioterrorism investigation. FDA Publishes Guidance for Bioterrorism Recordkeeping Requirements FDA announced the publication of a guidance document on the recordkeeping requirements of the Bioterrorism Act; the guidance topics include who must comply with and who is excluded from the rule, and what information is required to be kept and made available to FDA during a Bioterrorism investigation. NSF International to Host Training Seminar on Good Manufacturing Practices To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ. NSF International to Host Training Seminar on Good Manufacturing Practices To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ. NSF International to Host Training Seminar on Good Manufacturing Practices To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ. NSF International to Host Training Seminar on Good Manufacturing Practices To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ. NSF International to Host Training Seminar on Good Manufacturing Practices To help manufacturers interpret the new guidelines, NSF International will be hosting a GMP seminar on October 14, 2005 at the Sheraton Atlantic City Convention Center Hotel in Atlantic City, NJ. New AHPA FDA Inspection Guidance Available AHPA’s Guidance for Addressing FDA Inspections of Dietary Supplement Facilities is now available for purchase from AHPA’s online bookstore (http://www.ahpa.org/bookstore.htm). New AHPA FDA Inspection Guidance Available AHPA’s Guidance for Addressing FDA Inspections of Dietary Supplement Facilities is now available for purchase from AHPA’s online bookstore (http://www.ahpa.org/bookstore.htm). Three Cortislim Defendants to Give up $4.5 Million in Cash and Other Assets California-based Pinnacle Marketing Concepts, Inc. and its president, Thomas F. Cheng, and Shawn M. Talbott will give up $4.5 million in cash and other assets to settle Federal Trade Commission charges stemming from their roles in the marketing of CortiSlim and CortiStress; FTC’s litigation continues against four remaining defendants. Three Cortislim Defendants to Give up $4.5 Million in Cash and Other Assets California-based Pinnacle Marketing Concepts, Inc. and its president, Thomas F. Cheng, and Shawn M. Talbott will give up $4.5 million in cash and other assets to settle Federal Trade Commission charges stemming from their roles in the marketing of CortiSlim and CortiStress; FTC’s litigation continues against four remaining defendants. Three Cortislim Defendants to Give up $4.5 Million in Cash and Other Assets California-based Pinnacle Marketing Concepts, Inc. and its president, Thomas F. Cheng, and Shawn M. Talbott will give up $4.5 million in cash and other assets to settle Federal Trade Commission charges stemming from their roles in the marketing of CortiSlim and CortiStress; FTC’s litigation continues against four remaining defendants. AHPA Files Further Comments with FDA on NDI Process Organization's position is that in the case of an unprocessed herb or botanical, a single complete NDI notification is sufficient, but with semi-purified extracts of botanicals, the end product might be significantly different. "“Each manufacturer of such extracts should submit an NDI notification with the requisite safety information.” AHPA Files Further Comments with FDA on NDI Process Organization's position is that in the case of an unprocessed herb or botanical, a single complete NDI notification is sufficient, but with semi-purified extracts of botanicals, the end product might be significantly different. "“Each manufacturer of such extracts should submit an NDI notification with the requisite safety information.” Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Alliance Principle Ingredients Receives Approval for Melatonin Use in Dietary Supplements in Canada Alliance Principle Ingredients announced that it has received approval from the Natural Health Products Directorate, in Canada, for melatonin. This allows Canadian manufacturers using melatonin from Alliance Principle Ingredients to receive Natural Health Product Numbers (NPN’s) for its products containing the ingredient. Developer and Marketers of 'Supreme Greens with MSM' Settle FTC Charges Supreme Greens developer Alejandro Guerrero and his company, Health Solutions, Inc., and Michael Howell, Gregory Geremesz and their company, Healthy Solutions, LLC have settled Federal Trade Commission charges over their roles in the deceptive marketing of Supreme Greens herbal supplement. Developer and Marketers of 'Supreme Greens with MSM' Settle FTC Charges Supreme Greens developer Alejandro Guerrero and his company, Health Solutions, Inc., and Michael Howell, Gregory Geremesz and their company, Healthy Solutions, LLC have settled Federal Trade Commission charges over their roles in the deceptive marketing of Supreme Greens herbal supplement. AHPA Asks FDA, NCCAM to Portray Supplements Honestly Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively. AHPA Asks FDA, NCCAM to Portray Supplements Honestly Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively. AHPA Asks FDA, NCCAM to Portray Supplements Honestly Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively. AHPA Asks FDA, NCCAM to Portray Supplements Honestly Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively. AHPA Asks FDA, NCCAM to Portray Supplements Honestly Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively. AHPA Asks FDA, NCCAM to Portray Supplements Honestly Association challenges the FDA and the National Center for Complementary and Alternative Medicine to tell the truth and to correct past misstatements about dietary supplements and echinacea products, respectively. 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. NBTY, Inc. to Pay $2 Million Penalty For Alleged Violations of FTC Order Under the terms of a consent decree approved by the Federal Trade Commission, for submission by the U.S. Department of Justice to the federal court for approval, NBTY, Inc. will pay a $2 million civil penalty to settle charges that it violated the terms of a 1995 Commission order by making false and misleading health claims about two of its products - “Royal Tongan Limu" and “Body Success PM Diet Program”. NBTY, Inc. to Pay $2 Million Penalty For Alleged Violations of FTC Order Under the terms of a consent decree approved by the Federal Trade Commission, for submission by the U.S. Department of Justice to the federal court for approval, NBTY, Inc. will pay a $2 million civil penalty to settle charges that it violated the terms of a 1995 Commission order by making false and misleading health claims about two of its products - “Royal Tongan Limu" and “Body Success PM Diet Program”. Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December. Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December. Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December. Food Allergen Labeling Law Effective January 1 for All Foods and Dietary Supplements Any food (including dietary supplements) that contains a major food allergen must include specific warnings when labeled on or after January 1, 2006; AHPA to hold tele-seminar on the new requirement at the end of November, with a repeat session in early December. AER Amendment Dropped from Senate Defense Bill Following discussion on the Senate floor last week, Senator Richard Durbin (D-IL) won a commitment from the chairman of the Senate Health, Education, Labor and Pensions (HELP) Committee to prioritize efforts to pass legislation requiring supplement manufacturers to submit serious adverse event reports (AERs) to the Food and Drug Administration (FDA). AER Amendment Dropped from Senate Defense Bill Following discussion on the Senate floor last week, Senator Richard Durbin (D-IL) won a commitment from the chairman of the Senate Health, Education, Labor and Pensions (HELP) Committee to prioritize efforts to pass legislation requiring supplement manufacturers to submit serious adverse event reports (AERs) to the Food and Drug Administration (FDA). FDA Warns Companies To Stop Marketing Fruit Products With Unproven Disease Treatment and Prevention Claims The Food and Drug Administration (FDA) issued Warning Letters to 29 companies that manufacture, market, or distribute products made from cherries or other fruits, telling the firms to stop making unproven claims on the firms’ web sites and product labels that their fruit products treat or prevent disease. FDA Warns Companies To Stop Marketing Fruit Products With Unproven Disease Treatment and Prevention Claims The Food and Drug Administration (FDA) issued Warning Letters to 29 companies that manufacture, market, or distribute products made from cherries or other fruits, telling the firms to stop making unproven claims on the firms’ web sites and product labels that their fruit products treat or prevent disease. 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	US Food and Drug Administration Commissioner Lester Crawford has announced his resignation effective immediately. The move comes as a surprise after he was finally confirmed to the post by the Senate just two months ago. Crawford was previously agency deputy and acting commissioner before taking the top post. Health and Human Services Secretary Mike Leavitt accepted Crawford's resignation . According to the Associated Press, Dr. Andrew C. von Eschenbach has been tapped by President Bush as the temporary chief of the regulatory agency, saying that he will remain chief of the National Cancer Institute, the government's lead agency in researching cancer treatments, while running the FDA. Von Eschenbach gave no indication of whether he expected to be nominated as permanent chief.
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