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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
- Spectrum Organic Products Responds to FDA Letter Regarding Use of Non-GMO Seal on Canola Oil Label
- Supplement Group Targets Consumer Education
- Advanced Nutraceuticals, Inc. Announces 2001 Year End Results And Additional Financing
- ADM Awarded Nutraceuticals Patent Patent Creates Proprietary Position for ADM in Fast-Growing Nutraceutical Market
- Tantivy Sciences Obtains Exclusive License to Unique Nutraceutical Products
- Top GNC Executives Tour Pittsburgh Market to Present New Business Plan and Expansion Possibilities; Meeting will focus on new business strategies and growth
- Nutrition 21 Receives Patent For the Nutritional Treatment of Type 2 Diabetes; Patent Presents New Pharmaceutical Licensing Opportunities
- ConsumerLab.com Finds Most B-vitamin Supplements Contain What They Claim, But Often Exceed Safe Levels - Consumers Cautioned to Be Aware of Side Effects with High Dose Products
- Nutraceutix, Inc., Nutravite Announcement Commercial Availability of CDT™ Glucosamine for Canadian Marketplace
- Harvey Kamil Appointed President of NBTY, Inc. - Scott Rudolph to Continue as Chairman and CEO
- drugstore.com Expects to Reach Profitability Target in 2003
- Human Genome Project Leads to Innovative Healthcare
- NPIcenter’s Career Center targets nutraceutical Industry
- Adding Vitamin C To Certain Drugs May Help Treat Alzheimer's, Other Brain Disorders
- Adding Vitamin C To Certain Drugs May Help Treat Alzheimer's, Other Brain Disorders
- Editorial: An Exercise in Synergy
- NBTY, Inc. Appoints Harvey Kamil President, Scott Rudolph To Continue As Chairman And CEO
- Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids
- Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids
- Ross Products to Launch Infant Formula Supplemented With Two New Fatty Acids
- LignisulMSM vs Naproxen for Osteoarthritis Clinical Trial Gets Underway
- Natural Health Trends Corp. Launches Lexxus Taiwan
- FDA Presents Compliance Guide for Structure/Function Claims
- New TrimFit® Bars Redefine Energy Bar Category
- New TrimFit® Bars Redefine Energy Bar Category
- Probiata® Offers Safe, Natural and Effective Alternative
- Alive & Well with Michelle Harris
- Be Well and Get Rewarded! Find Personalized Wellness Solutions and Earn Free Vitamins at NatureMade.com
- Consumers Search for Healthy Cleaning Products That Work
- Nordic Naturals: Omega 3 Fatty Acids
- Cyanotech Names Bob Capelli as Director of Sales
- Report on the Codex Nutrition Committee Meeting in Bonn, Germany
Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting.
- Report on the Codex Nutrition Committee Meeting in Bonn, Germany
Particpants report little progress on key issues for the food supplements industry, with further substantive discussions to wait for the 2006 Thaaiand meeting.
- 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.
- Reparagen: From Concept to Product
Scientists have revealed a breakthrough in managing arthritis and joint damage. Published in BioMed Central’s BMC Complementary & Alternative Medicine, a natural product combination called Reparagen, has been shown to activate a critical repair gene, IGF-1, in human cartilage while blocking joint destruction associated with inflammation. This product was not originally created to specifically meet the needs of the joint health sector. Rather it is the result of a decade of research & development that was focused on the mechanism of action of the constituents. In this approach, elements of traditional knowledge are combined with new scientific discoveries, and novel ingredient combinations and applications can be created.
- Reparagen: From Concept to Product
Scientists have revealed a breakthrough in managing arthritis and joint damage. Published in BioMed Central’s BMC Complementary & Alternative Medicine, a natural product combination called Reparagen, has been shown to activate a critical repair gene, IGF-1, in human cartilage while blocking joint destruction associated with inflammation. This product was not originally created to specifically meet the needs of the joint health sector. Rather it is the result of a decade of research & development that was focused on the mechanism of action of the constituents. In this approach, elements of traditional knowledge are combined with new scientific discoveries, and novel ingredient combinations and applications can be created.
- Reparagen: From Concept to Product
Scientists have revealed a breakthrough in managing arthritis and joint damage. Published in BioMed Central’s BMC Complementary & Alternative Medicine, a natural product combination called Reparagen, has been shown to activate a critical repair gene, IGF-1, in human cartilage while blocking joint destruction associated with inflammation. This product was not originally created to specifically meet the needs of the joint health sector. Rather it is the result of a decade of research & development that was focused on the mechanism of action of the constituents. In this approach, elements of traditional knowledge are combined with new scientific discoveries, and novel ingredient combinations and applications can be created.
- Reparagen: From Concept to Product
Scientists have revealed a breakthrough in managing arthritis and joint damage. Published in BioMed Central’s BMC Complementary & Alternative Medicine, a natural product combination called Reparagen, has been shown to activate a critical repair gene, IGF-1, in human cartilage while blocking joint destruction associated with inflammation. This product was not originally created to specifically meet the needs of the joint health sector. Rather it is the result of a decade of research & development that was focused on the mechanism of action of the constituents. In this approach, elements of traditional knowledge are combined with new scientific discoveries, and novel ingredient combinations and applications can be created.
- Reparagen: From Concept to Product
Scientists have revealed a breakthrough in managing arthritis and joint damage. Published in BioMed Central’s BMC Complementary & Alternative Medicine, a natural product combination called Reparagen, has been shown to activate a critical repair gene, IGF-1, in human cartilage while blocking joint destruction associated with inflammation. This product was not originally created to specifically meet the needs of the joint health sector. Rather it is the result of a decade of research & development that was focused on the mechanism of action of the constituents. In this approach, elements of traditional knowledge are combined with new scientific discoveries, and novel ingredient combinations and applications can be created.
- Reparagen: From Concept to Product
Scientists have revealed a breakthrough in managing arthritis and joint damage. Published in BioMed Central’s BMC Complementary & Alternative Medicine, a natural product combination called Reparagen, has been shown to activate a critical repair gene, IGF-1, in human cartilage while blocking joint destruction associated with inflammation. This product was not originally created to specifically meet the needs of the joint health sector. Rather it is the result of a decade of research & development that was focused on the mechanism of action of the constituents. In this approach, elements of traditional knowledge are combined with new scientific discoveries, and novel ingredient combinations and applications can be created.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- European Parliament Passes Second Reading On Fortified Foods Regulations
The European Parliament voted yesterday on EU Fortified Foods Regulations yesterday, with the objective of laying down common EU rules on the addition of vitamins, minerals and other substances to foods. The rules will apply in 6 months, although for a period of three years afterwards, products not in compliance can be marketed, if they were labeled or placed into the market prior to the regulations coming into force. The regulations call for an approved list of vitamins and minerals, with others not on the list allowable if on the market at the time the regulations coming into force and use supported by dossiers to be transferred to the European Food Safety Authority (EFSA) for evaluation. The Comiology procedure, based on scientific advice from EFSA will be used for determining minimum and maximum levels.
- UK's MHRA to Require Label Warning on Black Cohosh
The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.”
- UK's MHRA to Require Label Warning on Black Cohosh
The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.”
- UK's MHRA to Require Label Warning on Black Cohosh
The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.”
- UK's MHRA to Require Label Warning on Black Cohosh
The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.”
- UK's MHRA to Require Label Warning on Black Cohosh
The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.”
- UK's MHRA to Require Label Warning on Black Cohosh
The Medicines and Healthcare products Regulatory Agency (MHRA) in the U.K. issued a press release today in which it stated that it “is concerned about links between black cohosh (Actaea racemosa; syn: Cimicifuga racemosa) and the risk of liver disorders. MHRA has therefore determined that warnings will be required on labeling of black cohosh products and it “is working with the herbal sector to ensure the public is fully informed about this potential risk.”
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- Accucaps Industries receives coveted certification from European Union (EU) for soft gel product line
Company has recently received European Union (EU) Certification enabling the company to export its products to any of the EU’s 25 member countries.
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- EAS Workshop: The Practical Implications of the EU's Nutrition and Health Claims Regulation
EAS is offering the opportunity to join a 'problem solving' workshop on the EU Regulations on nutrition and health claims and 'fortifed foods', September 13, 2006, at the Radisson Sas Royal Hotel, Brussels
- UK: Views Sought on Noni Juice Opinion
The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product.
- UK: Views Sought on Noni Juice Opinion
The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product.
- UK: Views Sought on Noni Juice Opinion
The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product.
- UK: Views Sought on Noni Juice Opinion
The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product.
- UK: Views Sought on Noni Juice Opinion
The expert scientific committee that advises the UK Food Standards Agency on novel foods is calling for comments on its draft opinion of a noni juice product.
- Baywood's Cal-Mag FIZZ Product Approved by European Union
Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries.
- Baywood's Cal-Mag FIZZ Product Approved by European Union
Company announces that its Cal-Mag FIZZ(TM) has been approved for marketing to the European Union (EU), a union of twenty-five independent member countries.
- 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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Earlier this week, the European Parliament held its second reading vote on proposed health and nutrition claims regulations, intended to ensure that consumers would be able to rely on the truth and accuracy of information on food labels and to create a level playing field for food manufacturers wishing to use health or nutrition claims. The second reading, which passed by an overwhelming majority, incorporated several amendments to the original proposed regulation, and is expected to be adopted by the European Council by this autumn, after which it will enter into force. The first provisions of the regulation will begin to apply 6 months from this time, and for those claims not specifically on the positive list, a transitional period of two years will apply for existing nutrition claims, three years for existing health claims.
The proposed Health and Nutrition Claims Regulation lays down strict conditions for the use of nutrition claims such as “low fat”, “high fibre” or “reduced sugar”. Set thresholds will have to be met before such claims can be made. For example, there will have to be 6g of fibre per 100g for the claim “high fibre” to be used and no more than 0.12g of sodium per 100g/100ml for the claim “low sodium/salt”. In addition, a nutrition claim can only be used if it fits a certain nutritional profile (i.e. below a certain salt, fat and/or sugar level). These nutritional profiles will be set by Commission and Member States through Comitology procedure, based on the opinion of the European Food Safety Authority (EFSA), within 24 months of the Regulation entering into force. A nutrition claim will still be permitted if only one nutrient (e.g. salt, sugar or fat) exceeds the limit of the nutritional profile. However, the high level of this substance must be clearly marked on the label, close to and with the same prominence as the claim.
Regarding health claims, the Commission will draw up a positive list of well-established health claims which may be used on a label so long as they are proven to apply to the food in question. Member States will submit a list of claims already approved at national level and, within 3 years of the Regulation entering into force, the Commission will produce an EU positive list of health claims. Any claims submitted for the EU list after this period will have to be examined by EFSA and approved by the Commission and Member States through the Comitology procedure. Further, the use of new health claims or disease reduction claims, such as “[name of product] lowers cholesterol” or “calcium helps reduce the risk of osteoporosis”, will require specific authorization, on a case by case basis, by the Commission through the Comitology procedure, following submission of a scientific dossier, involving scientific assessment and verification of the claim by the European Food Safety Authority (EFSA). In the simplified procedure envisioned, if the EFSA Opinion on the claim is positive, the Commission will take a decision on whether or not to authorize it after simple consultation of Members States. However, if EFSA gives a negative Opinion, the standard Comitology procedure will be used to decide whether or not to authorize the claim i.e. Member State experts will vote on a Commission proposal in the Standing Committee on the Food Chain and Animal Health.
The Regulation would apply to any food or drink product produced for human consumption to be sold on the EU/ Member States’ market. The proposed new rules do not cover cosmetics, medicine or pet food products.
Information in labeling, marketing or advertising about the nutritional or health benefits of foods which is not clear, accurate or substantiated will not be permitted. In addition, claims referring to rates or amounts of weight loss, as well as claims referring to recommendations of individual doctors will be banned. Health claims on alcoholic beverages above 1.2 % will also not be allowed, except those referring to a reduction in alcohol or energy content, due to the link between alcohol and other health and social problems.
More on Nutrient Profiles:
Nutrient profiles will be based on the scientific opinion of the European Food Safety Authority (EFSA). Within 24 months of the Regulation entering into force, the Commission will consult the relevant stakeholders, and present proposals for nutrient profiles to Member State experts in the Standing Committee on the Food Chain and Animal Health. If the Standing Committee backs these proposed nutrient profiles, they will be adopted by the Commission (Comitology procedure) and will enter into force following publication in the Official Journal of the European Communities. |