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- 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
- 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.
- Senate Confirms Crawford as FDA Commissioner
US Senate confirmed Lester Crawford, DVM, PhD, as FDA Commissioner
- Senate Confirms Crawford as FDA Commissioner
US Senate confirmed Lester Crawford, DVM, PhD, as FDA Commissioner
- Senate Confirms Crawford as FDA Commissioner
US Senate confirmed Lester Crawford, DVM, PhD, as FDA Commissioner
- Senate Confirms Crawford as FDA Commissioner
US Senate confirmed Lester Crawford, DVM, PhD, as FDA Commissioner
- CRN Applauds Confirmation Of Dr. Crawford As New FDA Commissioner
The Council for Responsible Nutrition (CRN), issued a statement in response to the confirmation of Lester Crawford, D.V.M., Ph.D., to the post of Food and Drug Administration (FDA) Commissioner.
- CRN Applauds Confirmation Of Dr. Crawford As New FDA Commissioner
The Council for Responsible Nutrition (CRN), issued a statement in response to the confirmation of Lester Crawford, D.V.M., Ph.D., to the post of Food and Drug Administration (FDA) Commissioner.
- CRN Applauds Confirmation Of Dr. Crawford As New FDA Commissioner
The Council for Responsible Nutrition (CRN), issued a statement in response to the confirmation of Lester Crawford, D.V.M., Ph.D., to the post of Food and Drug Administration (FDA) Commissioner.
- CRN Applauds Confirmation Of Dr. Crawford As New FDA Commissioner
The Council for Responsible Nutrition (CRN), issued a statement in response to the confirmation of Lester Crawford, D.V.M., Ph.D., to the post of Food and Drug Administration (FDA) Commissioner.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- Increased Demand For Astaxanthin to be Met By Fuji Health Science, Inc.
Company announces that it has successfully completed a New Dietary Ingredient (NDI) notification to the FDA under DSHEA for AstaREAL® astaxanthin produced at its facility in Gustavsberg, Sweden.
- AHPA Posts Revised Facts about Codex / EU Directive / CAFTA
document, “Codex Alimentarius and dietary supplements,” has now been revised to provide information on the current status of the European Union’s Directive on Vitamin and Mineral Supplements and to address emerging concerns related to CAFTA.
- AHPA Posts Revised Facts about Codex / EU Directive / CAFTA
document, “Codex Alimentarius and dietary supplements,” has now been revised to provide information on the current status of the European Union’s Directive on Vitamin and Mineral Supplements and to address emerging concerns related to CAFTA.
- AHPA Posts Revised Facts about Codex / EU Directive / CAFTA
document, “Codex Alimentarius and dietary supplements,” has now been revised to provide information on the current status of the European Union’s Directive on Vitamin and Mineral Supplements and to address emerging concerns related to CAFTA.
- AHPA Posts Revised Facts about Codex / EU Directive / CAFTA
document, “Codex Alimentarius and dietary supplements,” has now been revised to provide information on the current status of the European Union’s Directive on Vitamin and Mineral Supplements and to address emerging concerns related to CAFTA.
- NNFA Update: Echinacea Study Questioned/CAFTA Passed, Still No Threat
Association notes NEJM article on echinacea and questions dose used; observes that CAFTA passes with no impact on DSHEA's governing of the industry.
- NNFA Update: Echinacea Study Questioned/CAFTA Passed, Still No Threat
Association notes NEJM article on echinacea and questions dose used; observes that CAFTA passes with no impact on DSHEA's governing of the industry.
- NNFA Update: Echinacea Study Questioned/CAFTA Passed, Still No Threat
Association notes NEJM article on echinacea and questions dose used; observes that CAFTA passes with no impact on DSHEA's governing of the industry.
- NNFA Update: Echinacea Study Questioned/CAFTA Passed, Still No Threat
Association notes NEJM article on echinacea and questions dose used; observes that CAFTA passes with no impact on DSHEA's governing of the industry.
- NNFA Update: Echinacea Study Questioned/CAFTA Passed, Still No Threat
Association notes NEJM article on echinacea and questions dose used; observes that CAFTA passes with no impact on DSHEA's governing of the industry.
- NNFA Update: Echinacea Study Questioned/CAFTA Passed, Still No Threat
Association notes NEJM article on echinacea and questions dose used; observes that CAFTA passes with no impact on DSHEA's governing of the industry.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- Nutrition 21 Receives Widespread Approval in Europe for the Continued Sale of Chromax(R) Chromium Picolinate and Zinmax(R) Zinc Picolinate
Company has received "derogation" in more than 17 member states within the European Union (EU) for Chromax(R) chromium picolinate and Zinmax(R) zinc picolinate as ingredients and stand-alone brands.
- CRN Supports "Food Stamp" Bill
Associations, urges committee members to give strong consideration to a bill introduced last week by Senators Tom Harkin (D-Iowa) and Orrin Hatch (R-Utah), that would provide low-income households the opportunity to use their food stamps to purchase vitamin and mineral supplements.
- CRN Supports "Food Stamp" Bill
Associations, urges committee members to give strong consideration to a bill introduced last week by Senators Tom Harkin (D-Iowa) and Orrin Hatch (R-Utah), that would provide low-income households the opportunity to use their food stamps to purchase vitamin and mineral supplements.
- CRN Supports "Food Stamp" Bill
Associations, urges committee members to give strong consideration to a bill introduced last week by Senators Tom Harkin (D-Iowa) and Orrin Hatch (R-Utah), that would provide low-income households the opportunity to use their food stamps to purchase vitamin and mineral supplements.
- CRN Supports "Food Stamp" Bill
Associations, urges committee members to give strong consideration to a bill introduced last week by Senators Tom Harkin (D-Iowa) and Orrin Hatch (R-Utah), that would provide low-income households the opportunity to use their food stamps to purchase vitamin and mineral supplements.
- 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).
- 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.
- 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
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Food Standards Australia New Zealand (FSANZ) today released details of changes being considered to the Australia New Zealand Food Standards Codeand invited individuals and organisations with an interest in food standards to comment on the proposals.
The changes include the fortification of cereal-based beverages with selected vitamins and minerals, two new GM foods, the addition of phytosterols to fruit juices and fruit drinks, and an examination of benzoate and sulphite additives in food.
FSANZ is an independent government agency that sets food standards for Australia and New Zealand.
Industry can apply to FSANZ to vary food standards in the Code at any time. FSANZ’s responsibility is to ensure that changes are only approved if there are no concerns for public health and safety and that adequate and accurate information is provided to consumers.
The standard-setting process usually involves two rounds of public consultation. Information on how to make a submission can be found on the FSANZ website at www.foodstandards.gov.au.
Phytosterols in fruit juice and fruit juice drinks (Application A560 –Initial Assessment)
Coca-Cola South Pacific Pty Ltd has applied for permission to use phytosterols derived from vegetable oils as novel food ingredients in fruit juice and fruit drinks containing a minimum 20% fruit juice. The products are intended for consumers over the age of 40 with concerns about their blood cholesterol levels. Phytosterols are already allowed in table spreads and margarines and their use in low-fat milk, yoghurt and breakfast cereals is under consideration. Novel food ingredients such as phytosterols must undergo a safety assessment by FSANZ before they can be sold. FSANZ is seeking community comment at this early stage on a range of issues associated with the use of phytosterols in fruit juice and fruit juice drinks.
Phospholipase A1 as a processing aid (Application A561 –Initial Assessment)
Novozymes A/S has asked FSANZ to amend the Food Standards Code to approve the use of a new enzyme –phospholipase A1 –as a processing aid. Its purpose would be to improve process efficiencies and yields in cheese manufacture. The new enzyme is produced using recombinant DNA techniques. The related enzyme, phospholipase A2, has already been approved for use as a processing aid. We welcome comment on this application.
Food derived from insect-protected corn (Application 564 –Initial Assessment)
Syngenta Seeds Pty Ltd is seeking approval for food derived from corn line MIR604, which has been genetically modified to be resistant to three species of corn rootworm. If approved, food from this corn line will be able to enter Australia and New Zealand as imported products. The application is for use of MIR604 corn as a food only. At present, GM corn cannot be grown commercially in either country. If FSANZ accepts this application, it will undertake a safety assessment of the new GM corn to ensure that it is as safe for consumers as its non-GM counterpart.
Benzoate and sulphite permissions in food (Proposal P298 –Initial Assessment)
FSANZ is reviewing the use of sulphites and benzoates as chemical preservatives in food. The review has been initiated because the 21stAustralian Total Diet Study found high consumption levels by some age groups in the population, including young children. Although these high levels are unacceptable, they do not represent a risk to the health of these individuals. We intend to work with food manufacturers to establish the best way, if necessary, to reduce dietary exposure to sulphites and benzoates. We are seeking input to the review from concerned individuals, consumers, public health professionals and industry.
Fortification of cereal-based beverages (Application A500 –Draft Assessment)
So Natural Foods Australia has requested an amendment to the Food Standards Code to allow the addition of calcium to cereal-based beverages (eg rice and oat beverages). These beverages are generally consumed by individuals who are allergic/intolerant to dairy and/or soy products, or who choose not to consume dairy products. FSANZ has put forward three regulatory options for discussion, including its preferred option, which would permit the voluntary addition of selected vitamins and minerals to cereal-based beverages, with a requirement for specific advisory labelling. We welcome comment on this and the other strategies.
Food derived from glyphosate-tolerant cotton (Application 553 –Draft Assessment)
Monsanto Australia Limited has applied for approval for food derived from genetically modified cotton line MON 88913. The introduced genetic trait confers increased tolerance to glyphosate herbicide (Roundup Readyâ) during the reproductive phases of growth. All GM foods must undergo a pre-market safety assessment by FSANZ before they can be sold in Australia and New Zealand. FSANZ has concluded that there are no public health and safety issues associated with this GM cotton and is recommending approval for use, mainly as cottonseed oil.
Submissions: FSANZ welcomes public comment from industry, public health professionals, government agencies and consumers. Details of all the assessments above can be found on http://www.foodstandards.gov.au/mediareleasespublications/mediareleases/mediareleases2005/fsanzseekspubliccomm2967.cfm. Submissions close on 14 September 2005. |