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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
- EFSA Adopts First Opinions on Health Claims Made on Foods Relating to Disease Risk Reduction and Children's Health
EFSA’s Panel on dietetic products, nutrition and allergies (NDA) has adopted its first series of opinions on claims referring to the reduction of disease risk, and children's development and health. Scientists of the NDA Panel examined the scientific evidence for 8 claims, 5 of which related to children’s health and 3 to disease risk reduction.
- EFSA Adopts First Opinions on Health Claims Made on Foods Relating to Disease Risk Reduction and Children's Health
EFSA’s Panel on dietetic products, nutrition and allergies (NDA) has adopted its first series of opinions on claims referring to the reduction of disease risk, and children's development and health. Scientists of the NDA Panel examined the scientific evidence for 8 claims, 5 of which related to children’s health and 3 to disease risk reduction.
- EFSA Adopts First Opinions on Health Claims Made on Foods Relating to Disease Risk Reduction and Children's Health
EFSA’s Panel on dietetic products, nutrition and allergies (NDA) has adopted its first series of opinions on claims referring to the reduction of disease risk, and children's development and health. Scientists of the NDA Panel examined the scientific evidence for 8 claims, 5 of which related to children’s health and 3 to disease risk reduction.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- EU as a global exporter of regulation
Simon Pettman, Director of international food and nutrition policy consultancy EAS, said that EU efforts to harmonise regulations across its 27 member states has drawn interest across the globe, highlighting that in many areas including the food sector, Europe is fast becoming an exporter of regulation.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- Cognis Meets International Standard for Food Safety
The Cognis esterification plant at the Nutrition & Health Competence Center in Illertissen, Germany, has received the internationally renowned certificate of quality ISO 22000:2005 from the certification body DQS GmbH. The worldwide standard for food safety places rigorous demands on all process levels and along the whole chain of food production – from choosing raw materials and producing ingredients to manufacturing consumer products.
- New Director General for Canada's NHPD
As a result of a competitive process, Michelle Boudreau has been selected as Director General of the Natural Health Products Directorate (NHPD) effective September 8, 2008.
- New Director General for Canada's NHPD
As a result of a competitive process, Michelle Boudreau has been selected as Director General of the Natural Health Products Directorate (NHPD) effective September 8, 2008.
- New Director General for Canada's NHPD
As a result of a competitive process, Michelle Boudreau has been selected as Director General of the Natural Health Products Directorate (NHPD) effective September 8, 2008.
- New Director General for Canada's NHPD
As a result of a competitive process, Michelle Boudreau has been selected as Director General of the Natural Health Products Directorate (NHPD) effective September 8, 2008.
- New Director General for Canada's NHPD
As a result of a competitive process, Michelle Boudreau has been selected as Director General of the Natural Health Products Directorate (NHPD) effective September 8, 2008.
- New Director General for Canada's NHPD
As a result of a competitive process, Michelle Boudreau has been selected as Director General of the Natural Health Products Directorate (NHPD) effective September 8, 2008.
- Cantox to Host Educational Seminar Regarding Section 912: Potential Threat to Food Innovation
Cantox Health Sciences International will be hosting a seminar regarding Section 912, part of a law that includes prohibition that represents a shift in the dividing line between foods and drugs, and threatens to present significant hurdles for anyone involved in product development.
- Cantox to Host Educational Seminar Regarding Section 912: Potential Threat to Food Innovation
Cantox Health Sciences International will be hosting a seminar regarding Section 912, part of a law that includes prohibition that represents a shift in the dividing line between foods and drugs, and threatens to present significant hurdles for anyone involved in product development.
- Cantox to Host Educational Seminar Regarding Section 912: Potential Threat to Food Innovation
Cantox Health Sciences International will be hosting a seminar regarding Section 912, part of a law that includes prohibition that represents a shift in the dividing line between foods and drugs, and threatens to present significant hurdles for anyone involved in product development.
- Cantox to Host Educational Seminar Regarding Section 912: Potential Threat to Food Innovation
Cantox Health Sciences International will be hosting a seminar regarding Section 912, part of a law that includes prohibition that represents a shift in the dividing line between foods and drugs, and threatens to present significant hurdles for anyone involved in product development.
- Cantox to Host Educational Seminar Regarding Section 912: Potential Threat to Food Innovation
Cantox Health Sciences International will be hosting a seminar regarding Section 912, part of a law that includes prohibition that represents a shift in the dividing line between foods and drugs, and threatens to present significant hurdles for anyone involved in product development.
- Cantox to Host Educational Seminar Regarding Section 912: Potential Threat to Food Innovation
Cantox Health Sciences International will be hosting a seminar regarding Section 912, part of a law that includes prohibition that represents a shift in the dividing line between foods and drugs, and threatens to present significant hurdles for anyone involved in product development.
- FTC Sweep Stops Peddlers of Bogus Cancer Cures
The Federal Trade Commission has announced 11 law enforcement actions challenging deceptive advertising of bogus cancer cures. The FTC charged the companies with making unsupported claims that their products cured or treated one or more types of cancer. In each case, the company is charged with violating the FTC Act, which bars deceptive claims. Some complaints allege that the companies also falsely touted clinical or scientific proof for their products.
- FTC Sweep Stops Peddlers of Bogus Cancer Cures
The Federal Trade Commission has announced 11 law enforcement actions challenging deceptive advertising of bogus cancer cures. The FTC charged the companies with making unsupported claims that their products cured or treated one or more types of cancer. In each case, the company is charged with violating the FTC Act, which bars deceptive claims. Some complaints allege that the companies also falsely touted clinical or scientific proof for their products.
- FTC Sweep Stops Peddlers of Bogus Cancer Cures
The Federal Trade Commission has announced 11 law enforcement actions challenging deceptive advertising of bogus cancer cures. The FTC charged the companies with making unsupported claims that their products cured or treated one or more types of cancer. In each case, the company is charged with violating the FTC Act, which bars deceptive claims. Some complaints allege that the companies also falsely touted clinical or scientific proof for their products.
- FTC Sweep Stops Peddlers of Bogus Cancer Cures
The Federal Trade Commission has announced 11 law enforcement actions challenging deceptive advertising of bogus cancer cures. The FTC charged the companies with making unsupported claims that their products cured or treated one or more types of cancer. In each case, the company is charged with violating the FTC Act, which bars deceptive claims. Some complaints allege that the companies also falsely touted clinical or scientific proof for their products.
- FTC Sweep Stops Peddlers of Bogus Cancer Cures
The Federal Trade Commission has announced 11 law enforcement actions challenging deceptive advertising of bogus cancer cures. The FTC charged the companies with making unsupported claims that their products cured or treated one or more types of cancer. In each case, the company is charged with violating the FTC Act, which bars deceptive claims. Some complaints allege that the companies also falsely touted clinical or scientific proof for their products.
- FANCL Establishes Health Food Safety & Quality Standard
- FANCL Establishes Health Food Safety & Quality Standard
- FANCL Establishes Health Food Safety & Quality Standard
- FANCL Establishes Health Food Safety & Quality Standard
- FANCL Establishes Health Food Safety & Quality Standard
- FANCL Publishes Health Food Raw Materials’ Place of Origin on Website
- FANCL Publishes Health Food Raw Materials’ Place of Origin on Website
- FANCL Publishes Health Food Raw Materials’ Place of Origin on Website
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Sucralose Manufacturer Confirms United States ITC's Positive Initial Determination In Section 337 Sucralose Patent Infringement Investigation
Guangdong Food Industry Institute (GDFII/L&P Food) has announced that Administrative Law Judge Charles E. Bullock of the United States International Trade Commission (ITC) has determined that GDFII/L&P does not infringe any of the patents asserted by Tate & Lyle’s Section 337 complaint (docket# 337-TA-604). The complaint alleges infringement of process patents relating to the production of sucralose and certain intermediate compounds. This initial determination was presented by the US ITC September 22, 2008.
- Notice to OMB Reflects Industry Concerns About AER Labeling Financial Burden
The Natural Products Association has announced that the U.S. Food and Drug Administration (FDA) released a pre-publication notice of proposed collection of information to the Office of Management and Budget (OMB) for review in the pre-published Federal Register online. This submission follows the draft guidance titled “Dietary Supplement Labeling Requirements and Recommendations under the Dietary Supplement and Nonprescription Drug Consumer Protection Act,” which the agency published for comment January 2, 2008.
- Notice to OMB Reflects Industry Concerns About AER Labeling Financial Burden
The Natural Products Association has announced that the U.S. Food and Drug Administration (FDA) released a pre-publication notice of proposed collection of information to the Office of Management and Budget (OMB) for review in the pre-published Federal Register online. This submission follows the draft guidance titled “Dietary Supplement Labeling Requirements and Recommendations under the Dietary Supplement and Nonprescription Drug Consumer Protection Act,” which the agency published for comment January 2, 2008.
- Notice to OMB Reflects Industry Concerns About AER Labeling Financial Burden
The Natural Products Association has announced that the U.S. Food and Drug Administration (FDA) released a pre-publication notice of proposed collection of information to the Office of Management and Budget (OMB) for review in the pre-published Federal Register online. This submission follows the draft guidance titled “Dietary Supplement Labeling Requirements and Recommendations under the Dietary Supplement and Nonprescription Drug Consumer Protection Act,” which the agency published for comment January 2, 2008.
- Notice to OMB Reflects Industry Concerns About AER Labeling Financial Burden
The Natural Products Association has announced that the U.S. Food and Drug Administration (FDA) released a pre-publication notice of proposed collection of information to the Office of Management and Budget (OMB) for review in the pre-published Federal Register online. This submission follows the draft guidance titled “Dietary Supplement Labeling Requirements and Recommendations under the Dietary Supplement and Nonprescription Drug Consumer Protection Act,” which the agency published for comment January 2, 2008.
- Notice to OMB Reflects Industry Concerns About AER Labeling Financial Burden
The Natural Products Association has announced that the U.S. Food and Drug Administration (FDA) released a pre-publication notice of proposed collection of information to the Office of Management and Budget (OMB) for review in the pre-published Federal Register online. This submission follows the draft guidance titled “Dietary Supplement Labeling Requirements and Recommendations under the Dietary Supplement and Nonprescription Drug Consumer Protection Act,” which the agency published for comment January 2, 2008.
- HHS Preparing to Open FDA Offices in China, India, Europe, and Latin America This Year
The U.S. Department of Health and Human Services will send the first U.S. Food and Drug Administration (FDA) staff to China, India, Europe, and Latin America before the end of 2008, HHS Secretary Mike Leavitt has announced.
- HHS Preparing to Open FDA Offices in China, India, Europe, and Latin America This Year
The U.S. Department of Health and Human Services will send the first U.S. Food and Drug Administration (FDA) staff to China, India, Europe, and Latin America before the end of 2008, HHS Secretary Mike Leavitt has announced.
- HHS Preparing to Open FDA Offices in China, India, Europe, and Latin America This Year
The U.S. Department of Health and Human Services will send the first U.S. Food and Drug Administration (FDA) staff to China, India, Europe, and Latin America before the end of 2008, HHS Secretary Mike Leavitt has announced.
- HHS Preparing to Open FDA Offices in China, India, Europe, and Latin America This Year
The U.S. Department of Health and Human Services will send the first U.S. Food and Drug Administration (FDA) staff to China, India, Europe, and Latin America before the end of 2008, HHS Secretary Mike Leavitt has announced.
- HHS Preparing to Open FDA Offices in China, India, Europe, and Latin America This Year
The U.S. Department of Health and Human Services will send the first U.S. Food and Drug Administration (FDA) staff to China, India, Europe, and Latin America before the end of 2008, HHS Secretary Mike Leavitt has announced.
- New Certification Requirement for Certain Iron-Containing Dietary Supplements Effective Nov. 12, 2008
The “Consumer Product Safety Improvement Act of 2008” (15 U.S.C. § 2063(a)(1)) (CPSIA) requires that products subject to a consumer product safety rule include a Certificate of Compliance when shipped in commerce on and after Nov.12, 2008. For dietary supplement manufacturers, products subject to a consumer product safety rule are those that contain over 250 mg of elemental iron and are required to be in childproof closures by regulations promulgated under the “Poison Prevention Packaging Act,” a statute administered by the U.S. Consumer Product Safety Commission (CPSC).
- New Certification Requirement for Certain Iron-Containing Dietary Supplements Effective Nov. 12, 2008
The “Consumer Product Safety Improvement Act of 2008” (15 U.S.C. § 2063(a)(1)) (CPSIA) requires that products subject to a consumer product safety rule include a Certificate of Compliance when shipped in commerce on and after Nov.12, 2008. For dietary supplement manufacturers, products subject to a consumer product safety rule are those that contain over 250 mg of elemental iron and are required to be in childproof closures by regulations promulgated under the “Poison Prevention Packaging Act,” a statute administered by the U.S. Consumer Product Safety Commission (CPSC).
- New Certification Requirement for Certain Iron-Containing Dietary Supplements Effective Nov. 12, 2008
The “Consumer Product Safety Improvement Act of 2008” (15 U.S.C. § 2063(a)(1)) (CPSIA) requires that products subject to a consumer product safety rule include a Certificate of Compliance when shipped in commerce on and after Nov.12, 2008. For dietary supplement manufacturers, products subject to a consumer product safety rule are those that contain over 250 mg of elemental iron and are required to be in childproof closures by regulations promulgated under the “Poison Prevention Packaging Act,” a statute administered by the U.S. Consumer Product Safety Commission (CPSC).
- New Certification Requirement for Certain Iron-Containing Dietary Supplements Effective Nov. 12, 2008
The “Consumer Product Safety Improvement Act of 2008” (15 U.S.C. § 2063(a)(1)) (CPSIA) requires that products subject to a consumer product safety rule include a Certificate of Compliance when shipped in commerce on and after Nov.12, 2008. For dietary supplement manufacturers, products subject to a consumer product safety rule are those that contain over 250 mg of elemental iron and are required to be in childproof closures by regulations promulgated under the “Poison Prevention Packaging Act,” a statute administered by the U.S. Consumer Product Safety Commission (CPSC).
- New Certification Requirement for Certain Iron-Containing Dietary Supplements Effective Nov. 12, 2008
The “Consumer Product Safety Improvement Act of 2008” (15 U.S.C. § 2063(a)(1)) (CPSIA) requires that products subject to a consumer product safety rule include a Certificate of Compliance when shipped in commerce on and after Nov.12, 2008. For dietary supplement manufacturers, products subject to a consumer product safety rule are those that contain over 250 mg of elemental iron and are required to be in childproof closures by regulations promulgated under the “Poison Prevention Packaging Act,” a statute administered by the U.S. Consumer Product Safety Commission (CPSC).
- New Certification Requirement for Certain Iron-Containing Dietary Supplements Effective Nov. 12, 2008
The “Consumer Product Safety Improvement Act of 2008” (15 U.S.C. § 2063(a)(1)) (CPSIA) requires that products subject to a consumer product safety rule include a Certificate of Compliance when shipped in commerce on and after Nov.12, 2008. For dietary supplement manufacturers, products subject to a consumer product safety rule are those that contain over 250 mg of elemental iron and are required to be in childproof closures by regulations promulgated under the “Poison Prevention Packaging Act,” a statute administered by the U.S. Consumer Product Safety Commission (CPSC).
- 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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Health claims regulation across Asia and the European Union will come under the spotlight at an upcoming workshop hosted by international food and nutrition policy consultancy EAS.
The workshop ‘The Practical Implications of Claims Regulations and key steps to successfully accessing markets in Asia & Europe’, will guide companies through the current rules for health claims in key Asian markets and Europe.
Taking place in Kuala Lumpur, Malaysia, on Tuesday November 18, the event will also highlight the current and future opportunities and challenges for claims made on products in key Asian markets and across the European Union.
Leading the workshop Daniel Tsi, Regional Director of EAS Asia, and EAS Europe Adviser Miguel da Silva, will give an overview of global regulatory developments, health supplements and functional foods classification, and health claims and authorisation procedures in major Asian markets such as China, Taiwan, and Malaysia, and the European Union (EU).
“The current regulatory environment in Asia alone is diverse and challenging both for companies and regulatory authorities,” said Dr Tsi. “Participants at the workshop will get a clear picture of the different regulations and practices in key Asian markets and the European Union, and find out how to ensure their functional nutritional products avoid the common pitfalls when launching products in these markets.”
Dr Tsi will give an overview of the growing trend towards health claims regulation in the Asian region, highlighting developments at Codex Alimentarius level and health claims legislation in the United States. He will also discuss the status and future development of claims regulation within the Association of South East Asian Nations (ASEAN).
With Europe being the first region to harmonise nutrition and health claims regulations, Mr da Silva will clarify the EU framework, from the different types of claims, their definitions and conditions of use, and the role of the European Food Safety Authority (EFSA) in their authorisation. He will also address the many lessons learnt so far from the European regulations and provide guidance on how some of the challenges could be avoided in future.
For the full workshop programme or to register for the event, visit www.eas.asia, or email carissachin@eas.asia. |