This presentation will allow the reader to know about NSF international its history, mission, NSF Mark, role in Dietary supplements and Nutraceutical industries. It also give information on testing, inspection, certification of products.
NSF certification, Standard for dietary supplementAtul Bhombe
Manufacturers, regulators and consumers look to NSF International for the development of public health standards and certification programs that help protect the world’s food, water, consumer products and environment. NSF is a global, independent organization, our standards team facilitates development of public health standards, and our service teams test, audit and certify products and services
REGULATORY ASPECTS OF FOOD & NUTRACEUTICALS A GLOBALKapilKumar198
This presentation contains detailed information about the regulatory aspects of food and nutraceuticals a global prospective, which includes WHO guidelines on nutrition and NSF International.
NSF certification, Standard for dietary supplementAtul Bhombe
Manufacturers, regulators and consumers look to NSF International for the development of public health standards and certification programs that help protect the world’s food, water, consumer products and environment. NSF is a global, independent organization, our standards team facilitates development of public health standards, and our service teams test, audit and certify products and services
REGULATORY ASPECTS OF FOOD & NUTRACEUTICALS A GLOBALKapilKumar198
This presentation contains detailed information about the regulatory aspects of food and nutraceuticals a global prospective, which includes WHO guidelines on nutrition and NSF International.
Biosimilars
A biosimilar is a biological medicine highly similar to another already approved biological medicine (the 'reference medicine'). (A medicine whose active substance is made by a living organism.)
Biologicals
Biological medicines contain active substances from a biological source, such as living cells or organisms and are often produced by cutting-edge technology.
Biological medicinal product
Biological Medicinal Products, also known as biologics or biologicals, are medicinal products that are manufactured using biotechnology processes and derived from living organisms or their products. They can include vaccines, blood products, gene therapies, monoclonal antibodies, recombinant proteins, and other complex biological substances.
Biological Investigational Medicinal Product
Refer to biological products that are being investigated in clinical trials or research studies to evaluate their safety, efficacy, or pharmacokinetic properties. These products have not yet received marketing authorization and are still in the experimental phase.
In the European Union, A biological substance is referred as the active ingredient in biological products.
A "biological substance" is defined as "a substance that is produced by or extracted from a biological source
That requires a combination of physico-chemical-biological testing, along with the production process and its control, for its characterization and the determination of its quality.“
Examples: Immunologic medicines
Medicines derived from human blood and plasma
Medicines developed by means of recombinant DNA technology
Hybridoma and mAb methods
Advanced therapy medicinal products
The requirements of the EU centralized procedure.
The approval standards for biotechnology products are the same as for chemically synthesized medicines.
Both types of products must be safe and effective and have appropriate quality.
MAA for a biotechnology product must meet the standard dossier submission requirements
MAA must generally comply with the CTD format, including with respect to
Module I (administrative information, including labelling)
Module 2 (various summaries)
Module 3 (chemical, pharmaceutical, and biological information)
Module 4 (nonclinical reports)
Module 5 (clinical study reports)
The EU has approved the highest number of biosimilars worldwide, and consequently has the most extensive experience of their use and safety.
EMA has issued scientific guidelines to help developers conform to the strict regulatory requirements for approving biosimilars.
The guidelines have evolved to keep pace with rapid advances in biotechnology and analytical sciences, and they take on board increasing experience of clinical use.
All medicines produced using biotechnology and those for specific indications must be approved in the EU through EMA
Some biosimilars may be approved at national level, such as some low-molecular weight heparins derived from porcine intestinal mucosa.
plasma master file is a EU requirement for the apploval of the biologics or the biosimilars to the EU in a eCTD format or Nees as per the requirement type and should contain the above given details
Herbal products, also known as botanical products or phytomedicines, are products made from plants to treat diseases or maintain health.
Herbal products are made by extracting active ingredients from plant parts, such as leaves, bark, roots, seeds, or flowers.
Herbal products, including dietary supplements, are regulated by the FDA. However, unlike pharmaceutical drugs, they do not require pre-market approval. Instead, manufacturers are responsible for ensuring the quality and safety of their products.
The FDA establishes Good Manufacturing Practices (GMP) regulations for dietary supplements to ensure quality control during manufacturing.
The safety of herbal products in the USA is overseen by various regulatory agencies, primarily the Food and Drug Administration (FDA) and the Federal Trade Commission (FTC).
To ensure a high degree of safety and effectiveness of herbal products and quality control standards during the manufacturing of herbal supplements and medicines, AHPA published GACP (Good Agriculture and Collection Practices) guideline in the American Herbal Pharmacopoeia.
The slides explain 21 CFR Part 812. It includes all the guidelines to be followed by any manufacturer and investigator while manufacturing and investigating the safety, efficacy of the medical device.
DIETARY SUPPLEMENT
The purpose of dietary supplements, is to enhance or supplement the diet. Even though a product is marketed as a dietary supplement, it is still considered a medicine to the extent that it is meant to treat, diagnose, cure, or prevent diseases.
Tablets, capsules, soft gels, powders, bars, gummies, and liquid supplements are just a few of the many different forms that supplements can take.
It is a product that is intended to supplement the diet that bears or contains one or more of the following dietary ingredients: a vitamin, a mineral, an herb or other botanical, an amino acid.
A dietary substance use by human to supplement the diet by increasing the total daily intake, or a concentrate, metabolite, constituent, extract, or combinations of these ingredients.
FDA Role
Companies can often introduce a dietary supplement to the market without notifying FDA.
FDA’s role in regulating dietary supplements primarily begins after products enter the marketplace.
If a product is found to be unsafe or not otherwise in compliance with the law, FDA can work with the company to bring the product into compliance or possibly remove it from the market.
FDA regulates both finished dietary supplement products and dietary ingredients.
FDA regulates dietary supplements under a different set of regulations than those covering "conventional" foods (edible fruits and vegetables) and drug products.
Role of DSHEA
Manufacturers and distributors of dietary supplements and dietary ingredients are prohibited from marketing products that are adulterated or misbranded.
That means that these firms are responsible for evaluating the safety and labelling of their products before marketing to ensure that they meet all the requirements of the Federal Food, Drug, and Cosmetic Act (FFDCA) as amended by DSHEA and FDA regulations.
FDA has the authority to take action against any adulterated or misbranded dietary supplement product after it reaches the market
The Dietary Supplement Health and Education Act of 1994 was enacted to prohibit
Dietary supplement manufacturers and distributors from making false claims (such as "natural" and "therapeutic," on supplement labels)
The law also prohibits the manufacture and sale of adulterated dietary supplements.
Aim of these act:
To make dietary supplements safer by forbidding manufacturers and distributors from producing and selling mislabelled or adulterated products.
Act requires that the manufacturer of the dietary supplement ensures their product meets DSHEA and FDA regulations.
Table of Contents
Short Title Reference Table Of Contents
Findings
Definitions
Safety of Dietary Supplements and Burden of Proof on FDA
Dietary Supplement Claims
Statements of Nutritional Support
Dietary supplement ingredient labeling and nutrition information labeling
New dietary ingredients
Good manufacturing practices
Conforming amendments
Withdrawal of the regulations and notice
Commission on dietary supplement labels
Introduction
Definition
Classification
Regulatory registration procedure
Quality system requirements
Clinical evaluation
Investigation of medical devices
Summary
Medical devices are regulated by the National Medical Product Administration (NMPA), formerly the China Food and Drug Administration (CFDA)
Manufacturers must register their devices with the NMPA before selling or distributing in China.
The NMPA reviews all device applications and has strict requirements for submission documentation, testing, and clinical data.
Any instrument, apparatus, appliance, material, or other article whether used alone or in combination, including the software necessary for its proper application.
Diagnosis, prevention, monitoring, treatment or alleviation of disease
Diagnosis, monitoring, treatment, alleviation of compensation for an injury or handicap conditions
Investigation, replacement or modification for anatomy or a physiological process
Control of conception
The Chinese authorities (CFDA/NMPA) have their own quality management system requirements.
However, these “GMP requirements” are very similar to ISO 13485.
Therefore, manufacturers usually submit the ISO 13485 certificate.
However, the audit will review this certificate against the Chinese GMP requirements.
These audits are regularly carried out during the approval procedure and/or after a recall.
NMPA issued and implemented the "Guideline on Inspection of Quality Management System for Medical Device Registration" on October 10, 2022.
Product Life-cycle Process
The guideline specifies the basic requirements for registration inspection, self-inspection, commissioned inspection, and extended inspection, etc. Applicant needs to:
Ensure the design, development, production, and other process data to be true, accurate, complete, and traceable, and consistent with the registration application materials.
Carry out the registration QMS inspection in reference to the registration application materials, and focus on the design, development, procurement, production management, and quality control of the product.
For lower-risk medical devices (Class I and Class II), clinical evaluation may not always be required. However, higher-risk devices (Class III and implantable devices) generally require clinical evaluation.
The evaluation involves reviewing existing clinical data, scientific literature, and relevant clinical research to assess the safety and performance of the device.
All clinical trials for medical devices must follow China Good Clinical Practices
Clinical investigations are required if no equivalent devices can be found and safety and efficacy cannot be proven with other clinical and non-clinical data.
For certain medical devices, the NMPA may require clinical investigations, especially for novel devices or those with significant risk.
Clinical investigations involve conducting studies on human subjects to generate clinical data on the safety and effectiveness of the device.
plasma master file in European countries and requirements in letter of intent...Sanjay batra
it includes that what is plasma master file, principles, procedure to file PMF, strategy involved, administration information, certification procedure & inspection
NSF was founded in 1944 as the National Sanitation Foundation to help standardize sanitation and food safety at a time when the United States had no national sanitation standards.
Today, NSF is a global organization offering services in more than 170 countries. Headquartered in Ann Arbor, Michigan, United states.
NSF has more than 140 currently active public health standards and independent testing protocols.
The National Sanitation Foundation (NSF) is a non-profit organization that develops standards and certification programs for various industries, including the food and dietary supplements industry.
In the context of food and dietary supplements, NSF has developed several standards and certification programs to ensure product safety, quality, and compliance with regulatory requirements.
Biosimilars
A biosimilar is a biological medicine highly similar to another already approved biological medicine (the 'reference medicine'). (A medicine whose active substance is made by a living organism.)
Biologicals
Biological medicines contain active substances from a biological source, such as living cells or organisms and are often produced by cutting-edge technology.
Biological medicinal product
Biological Medicinal Products, also known as biologics or biologicals, are medicinal products that are manufactured using biotechnology processes and derived from living organisms or their products. They can include vaccines, blood products, gene therapies, monoclonal antibodies, recombinant proteins, and other complex biological substances.
Biological Investigational Medicinal Product
Refer to biological products that are being investigated in clinical trials or research studies to evaluate their safety, efficacy, or pharmacokinetic properties. These products have not yet received marketing authorization and are still in the experimental phase.
In the European Union, A biological substance is referred as the active ingredient in biological products.
A "biological substance" is defined as "a substance that is produced by or extracted from a biological source
That requires a combination of physico-chemical-biological testing, along with the production process and its control, for its characterization and the determination of its quality.“
Examples: Immunologic medicines
Medicines derived from human blood and plasma
Medicines developed by means of recombinant DNA technology
Hybridoma and mAb methods
Advanced therapy medicinal products
The requirements of the EU centralized procedure.
The approval standards for biotechnology products are the same as for chemically synthesized medicines.
Both types of products must be safe and effective and have appropriate quality.
MAA for a biotechnology product must meet the standard dossier submission requirements
MAA must generally comply with the CTD format, including with respect to
Module I (administrative information, including labelling)
Module 2 (various summaries)
Module 3 (chemical, pharmaceutical, and biological information)
Module 4 (nonclinical reports)
Module 5 (clinical study reports)
The EU has approved the highest number of biosimilars worldwide, and consequently has the most extensive experience of their use and safety.
EMA has issued scientific guidelines to help developers conform to the strict regulatory requirements for approving biosimilars.
The guidelines have evolved to keep pace with rapid advances in biotechnology and analytical sciences, and they take on board increasing experience of clinical use.
All medicines produced using biotechnology and those for specific indications must be approved in the EU through EMA
Some biosimilars may be approved at national level, such as some low-molecular weight heparins derived from porcine intestinal mucosa.
plasma master file is a EU requirement for the apploval of the biologics or the biosimilars to the EU in a eCTD format or Nees as per the requirement type and should contain the above given details
Herbal products, also known as botanical products or phytomedicines, are products made from plants to treat diseases or maintain health.
Herbal products are made by extracting active ingredients from plant parts, such as leaves, bark, roots, seeds, or flowers.
Herbal products, including dietary supplements, are regulated by the FDA. However, unlike pharmaceutical drugs, they do not require pre-market approval. Instead, manufacturers are responsible for ensuring the quality and safety of their products.
The FDA establishes Good Manufacturing Practices (GMP) regulations for dietary supplements to ensure quality control during manufacturing.
The safety of herbal products in the USA is overseen by various regulatory agencies, primarily the Food and Drug Administration (FDA) and the Federal Trade Commission (FTC).
To ensure a high degree of safety and effectiveness of herbal products and quality control standards during the manufacturing of herbal supplements and medicines, AHPA published GACP (Good Agriculture and Collection Practices) guideline in the American Herbal Pharmacopoeia.
The slides explain 21 CFR Part 812. It includes all the guidelines to be followed by any manufacturer and investigator while manufacturing and investigating the safety, efficacy of the medical device.
DIETARY SUPPLEMENT
The purpose of dietary supplements, is to enhance or supplement the diet. Even though a product is marketed as a dietary supplement, it is still considered a medicine to the extent that it is meant to treat, diagnose, cure, or prevent diseases.
Tablets, capsules, soft gels, powders, bars, gummies, and liquid supplements are just a few of the many different forms that supplements can take.
It is a product that is intended to supplement the diet that bears or contains one or more of the following dietary ingredients: a vitamin, a mineral, an herb or other botanical, an amino acid.
A dietary substance use by human to supplement the diet by increasing the total daily intake, or a concentrate, metabolite, constituent, extract, or combinations of these ingredients.
FDA Role
Companies can often introduce a dietary supplement to the market without notifying FDA.
FDA’s role in regulating dietary supplements primarily begins after products enter the marketplace.
If a product is found to be unsafe or not otherwise in compliance with the law, FDA can work with the company to bring the product into compliance or possibly remove it from the market.
FDA regulates both finished dietary supplement products and dietary ingredients.
FDA regulates dietary supplements under a different set of regulations than those covering "conventional" foods (edible fruits and vegetables) and drug products.
Role of DSHEA
Manufacturers and distributors of dietary supplements and dietary ingredients are prohibited from marketing products that are adulterated or misbranded.
That means that these firms are responsible for evaluating the safety and labelling of their products before marketing to ensure that they meet all the requirements of the Federal Food, Drug, and Cosmetic Act (FFDCA) as amended by DSHEA and FDA regulations.
FDA has the authority to take action against any adulterated or misbranded dietary supplement product after it reaches the market
The Dietary Supplement Health and Education Act of 1994 was enacted to prohibit
Dietary supplement manufacturers and distributors from making false claims (such as "natural" and "therapeutic," on supplement labels)
The law also prohibits the manufacture and sale of adulterated dietary supplements.
Aim of these act:
To make dietary supplements safer by forbidding manufacturers and distributors from producing and selling mislabelled or adulterated products.
Act requires that the manufacturer of the dietary supplement ensures their product meets DSHEA and FDA regulations.
Table of Contents
Short Title Reference Table Of Contents
Findings
Definitions
Safety of Dietary Supplements and Burden of Proof on FDA
Dietary Supplement Claims
Statements of Nutritional Support
Dietary supplement ingredient labeling and nutrition information labeling
New dietary ingredients
Good manufacturing practices
Conforming amendments
Withdrawal of the regulations and notice
Commission on dietary supplement labels
Introduction
Definition
Classification
Regulatory registration procedure
Quality system requirements
Clinical evaluation
Investigation of medical devices
Summary
Medical devices are regulated by the National Medical Product Administration (NMPA), formerly the China Food and Drug Administration (CFDA)
Manufacturers must register their devices with the NMPA before selling or distributing in China.
The NMPA reviews all device applications and has strict requirements for submission documentation, testing, and clinical data.
Any instrument, apparatus, appliance, material, or other article whether used alone or in combination, including the software necessary for its proper application.
Diagnosis, prevention, monitoring, treatment or alleviation of disease
Diagnosis, monitoring, treatment, alleviation of compensation for an injury or handicap conditions
Investigation, replacement or modification for anatomy or a physiological process
Control of conception
The Chinese authorities (CFDA/NMPA) have their own quality management system requirements.
However, these “GMP requirements” are very similar to ISO 13485.
Therefore, manufacturers usually submit the ISO 13485 certificate.
However, the audit will review this certificate against the Chinese GMP requirements.
These audits are regularly carried out during the approval procedure and/or after a recall.
NMPA issued and implemented the "Guideline on Inspection of Quality Management System for Medical Device Registration" on October 10, 2022.
Product Life-cycle Process
The guideline specifies the basic requirements for registration inspection, self-inspection, commissioned inspection, and extended inspection, etc. Applicant needs to:
Ensure the design, development, production, and other process data to be true, accurate, complete, and traceable, and consistent with the registration application materials.
Carry out the registration QMS inspection in reference to the registration application materials, and focus on the design, development, procurement, production management, and quality control of the product.
For lower-risk medical devices (Class I and Class II), clinical evaluation may not always be required. However, higher-risk devices (Class III and implantable devices) generally require clinical evaluation.
The evaluation involves reviewing existing clinical data, scientific literature, and relevant clinical research to assess the safety and performance of the device.
All clinical trials for medical devices must follow China Good Clinical Practices
Clinical investigations are required if no equivalent devices can be found and safety and efficacy cannot be proven with other clinical and non-clinical data.
For certain medical devices, the NMPA may require clinical investigations, especially for novel devices or those with significant risk.
Clinical investigations involve conducting studies on human subjects to generate clinical data on the safety and effectiveness of the device.
plasma master file in European countries and requirements in letter of intent...Sanjay batra
it includes that what is plasma master file, principles, procedure to file PMF, strategy involved, administration information, certification procedure & inspection
NSF was founded in 1944 as the National Sanitation Foundation to help standardize sanitation and food safety at a time when the United States had no national sanitation standards.
Today, NSF is a global organization offering services in more than 170 countries. Headquartered in Ann Arbor, Michigan, United states.
NSF has more than 140 currently active public health standards and independent testing protocols.
The National Sanitation Foundation (NSF) is a non-profit organization that develops standards and certification programs for various industries, including the food and dietary supplements industry.
In the context of food and dietary supplements, NSF has developed several standards and certification programs to ensure product safety, quality, and compliance with regulatory requirements.
Food quality control in the food industry is the process of monitoring and verifying food product quality throughout the supply chain1. The ultimate goal is to verify that products meet stringent criteria for safety, taste, appearance, and other factors1. Key procedures in food quality control include2:
Product & Recipe Formulation
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NSF International and its role in Dietary supplements & Nutraceutical industries.pptx
1. NSF International Its role in Dietary
supplements and Nutraceutical Industries.
Presented By: Under the Guidance of:
Syed Arshiya Mrs.M.Beena Devi
Y22MPH02043 M.Pharmacy
I/II M.Pharmacy(2nd Semester) Assistant professor
Department of Department of
Pharmaceutical Regulatory Affairs Pharmaceutical Regulatory Affairs
HINDU COLLEGE OF PHARMACY
Amaravati Road, Guntur – 522002, A.P, INDIA
2. Contents:
Introduction to NSF.
History.
Mission.
The NSF Mark.
NSF International role in Dietary supplements and Nutraceutical
Industries.
NSF services.
References.
2
3. INTRODUCTION
NSF stands for National Sanitation Foundation.
NSF is a product testing, inspection, certification organization.
HISTORY
• NSF International was founded in 1944 from the University of
Michigan's School of Public Health as the National Sanitation
Foundation (NSF) to standardize sanitation and food safety
requirements.
• Today, NSF is a global organization offering services in more than 170
countries. Headquartered in Ann Arbor, Michigan, remain committed
to protecting and improving human health worldwide.
3
4. • NSF developed first standards for the sanitation of soda fountain and
luncheonette equipment in the early 1950s by which NSF International
developed.
• In 2022, NSF changed it’s name from NSF International to NSF,
simplifying it for greater consistency between it’s global approach and
brand name.
• NSF has more than 140 currently active public health standards and
independent testing protocols. They address products ranging from
home water treatment systems to kitchen and household appliances to
dietary supplements to sustainable flooring and furnishings.
4
5. Highlights of History
1944
Walter Snyder, Henry Vaughan and Nathan Sinai found the
National Sanitation Foundation (NSF) in the University of
Michigan School of Public Health.
1952
NSF establishes the Council of Public Health Consultants.
Introducing NSF Standards 1 and 2, the first food equipment
standards.
1960
Standard 9 is developed, and the pool, spa and hot tub products
certification programme begins.
5
6. 1965
The plastics piping and wastewater treatment programme begin.
1967
NSF Testing Laboratories becomes a not-for-profit corporation.
1980
NSF develops the first national standard for water treatment chemicals
(NSF 61) following the passage of the Safe Drinking Water Act.
1984
The bottled water programme begins.
Establishes the Health Advisory Board.
6
7. 1991
Our ISO 9000 programme begins.
Receive accreditation by the American National Standards Institute
(ANSI).
1996
NSF-ISR is established as a wholly owned subsidiary of NSF.
NSF is designated a Collaborating Center on Drinking Water Safety and
Treatment by the World Health Organization (WHO).
1999
Establish the Center for Public Health Education at NSF.
7
8. 2002
Introduce a dietary supplement GMP (Good Manufacturing Practice)
registration programme.
2003
NSF develops NSF/ANSI 173, the first American National Standard for
dietary supplements.
2010
NSF launches a certification programme to verify the quality, safety and
performance of automotive aftermarket parts.
2011
Introduce a home product certification programme to test and certify
home kitchen products and appliances.
8
9. 2014
NSF introduces a cosmetics programme, providing cosmetic
manufacturers with auditing, training, product testing and certification
services.
MISSION
Since 1944, NSF’s mission has been to improve human and planet
health. Businesses, regulators and consumers look for NSF to facilitate
the development of public health standards and to provide services that
help protect food, water, consumer products and the environment.
9
10. The NSF Mark
• The NSF mark is your assurance that the product has been tested by
one of the most respected independent certification organisations in
existence today. It is valued by consumers, manufacturers, retailers
and regulatory agencies worldwide.
10
11. • The NSF mark is specific to the type of product it appears on — from
dietary supplements, to water filters and dishwashers to plumbing
components, pool equipment and more.
• Products bearing an NSF certification mark meet all standard
requirements, including product testing and regular inspections to
verify products continue to comply with the standard.
Importance of NSF Mark
• Provides assurance that a product was impartially reviewed to
established standards or guidelines.
• Confirms that product labelling and claims have been objectively
verified by a trusted third party.
11
12. • Differentiates a product from the competition, offering a market
advantage.
• Demonstrates an organisation’s commitment to quality, compliance
and safety.
• Is backed by a team of professionals dedicated to public health and
safety operating in more than 180 countries.
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13. NSF International role in Dietary supplements and
Nutraceutical Industries.
• The term “Nutraceuticals” is the combination of the two words
“Nutrition” and “Pharmaceutical” coined by Stephen DeFelice.
• Nutraceuticals are a class of products that combine the benefits of both
nutrition and pharmaceuticals.
• According to DeFelice, Nutraceutical can be defined as, "a food (or
part of a food) that provides medical or health benefits, including
the prevention and/or treatment of a disease.
• These substances can include vitamins, minerals, amino acids,
enzymes, herbal extracts, and other bioactive compounds.
• Nutraceuticals are typically consumed in the form of dietary
supplements, functional foods, or fortified beverages.
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14. • The term “Dietary Supplement” wasn’t officially defined in the United
States until 1994 when the Dietary Supplement Health and Education Act
(DSHEA) was passed by Congress.
• DHSEA definition of a dietary supplement: “a vitamin, a mineral, an herb or
other botanical, an amino acid, a dietary substance for use by man to
supplement the diet by increasing the total dietary intake; or a concentrate,
metabolite, constituent, extract, or combination of any ingredient.”
• Dietary supplements include such ingredients as vitamins, minerals, herbs,
amino acids, and enzymes.
• Dietary supplements are marketed in forms such as tablets, capsules, soft
gels, gel caps, powders, and liquids.
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15. NSF Services
The services provided by NSF are:
Auditing
Certification
Consulting
Information Security
Sustainability
Training and Education
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16. Auditing
• Demonstrate the effectiveness of the organisation’s processes and
systems — and build confidence in the daily operations — with NSF
auditing services.
• Auditing the sectors like:
Food and Beverage
Health Sciences
Water
Management system
Building and construction
Automotive and aerospace
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17. Certification
• Demonstrate the organization’s compliance — and build consumer and
industry confidence — with NSF certification.
• Certification is provided for:
Food and Beverage
Health Sciences
Water
Management system
Building and construction
Automotive and aerospace
Sustainability
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18. NSF/ANSI 173 Certification
• NSF certifies dietary supplements to NSF/ANSI 173, the only
American National Standard for testing and certifying dietary
supplements.
• NSF evaluates the composition of dietary supplements and
ingredients. The assessment includes testing for vitamins, minerals,
herbs, botanicals, amino acids, sports supplements, concentrates,
metabolites, constituents and extracts to verify the product’s
contents accurately depicts its identity and purity specifications.
• To ensure that a safer product reaches consumers, we assess products
and ingredients for the presence of contaminants that impact health,
including the toxic elements lead, mercury, arsenic, cadmium and
chromium (VI).
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19. • Test for the presence of aerobic microorganisms, yeast and molds, and
Enterobacteriaceae, and specifically for the potential pathogens
Salmonella spp., Escherichia coli and Staphylococcus aureus.
• Analysis of mycotoxins, which are released by fungi and are
hepatotoxic.
• Assess items that contain botanical materials for the presence of
pesticides.
• Along with certification programme, conduction of annual audits and
periodically retest certified products to ensure continued compliance
with the most rigorous quality standard in the world for dietary
supplements.
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20. Third-Party Certification
Third-party certification means that an independent organisation has
reviewed the manufacturing process of a product and has independently
determined that the final product complies with specific standards for
safety, quality or performance.
Certification process:
Submit an
application
Undergo an
inspection
Get ready
for
certification
Comply
with regular
retesting
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21. Consulting
NSF provides cost-effective, world-class strategic and technical
consulting and training customized to your specific challenges and
needs.
Training and Education
As public health and safety standards evolve around the world,
companies must make sure their employees receive essential education
and training to stay ahead of the curve.
Sustainability
Through our standards, certification and auditing services, NSF can
support your company-wide sustainability strategies, allowing you to
open new business opportunities, pursue efficiency gains, save money
and attract and retain employees, customers and investors.
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