Therefore, we need to know which products are officially certified products, not pseudo-nutritional supplements with only QS logo.
At present, the only common official certification in China is "police mobile force", and the blue hat product is a health food mark approved by the US Food and Drug Administration.
FDA is the abbreviation of US Food and Drug Administration. The FDA sometimes represents the FDA of the United States, that is, the US Food and Drug Administration. The FDA of the United States is the authoritative organization of international medical audit, authorized by the US Congress, that is, the federal government, and is the highest law enforcement agency specializing in food and drug management; It is a government health control monitoring institution composed of doctors, lawyers, microbiologists, pharmacologists, chemists and statisticians, and is committed to protecting, promoting and improving national health. Many other countries seek and accept the help of FDA to promote it.
Significance of certification
At present, food, medicine, cosmetics, medical devices and other products that have passed FDA certification are globally recognized as products that are effective for human body and can ensure safety, and are the highest standards of product quality and effect in the world.
The FDA of the United States belongs to the Public Health Service Department of the State Council Health Service Department, and is responsible for managing all foods, medicines, cosmetics and radioactive instruments in the United States. It is also the earliest consumer protection agency in the United States. The FDA not only collects and processes 80,000 samples of products manufactured or imported in the United States for inspection, but also sends thousands of inspectors to overseas15,000 factories every year to confirm whether its activities comply with American laws and regulations.
Since 1990, the FDA of the United States has worked closely with international organizations such as ISO to continuously promote a series of innovative measures. Especially in the field of food and medicine, FDA certification has become the highest testing standard for food and medicine in the world. It is the highest food safety standard recognized by the World Health Organization. Only after the declared product is used in human body, it has been monitored at 143 key inspection points, and 20,000-30,000 people have been monitored for 3-7 years, then FDA certification will be issued. Therefore, many international manufacturers regard the pursuit of FDA certification as the highest honor and guarantee of product quality.
FDA's international free sales license is not only the highest level of FDA certification in the United States, but also the highest level of food and drug certification recognized by the World Trade Organization (WTO). This is the only certification, which can only be issued after it has been fully approved by FDA and WTO. Once this certification is obtained, the products can smoothly enter any WTO member country, even the marketing method, and the host government shall not interfere.
FDA has great influence in the United States and even the world, and is known as "the patron saint of American health". Drug dealers and food vendors all over the world love and fear it, and its reputation and professional standards have won the trust of many experts and the general public. While providing good protection, its strict testing and evaluation has also caused many drug dealers and food dealers to criticize it for hindering invention and innovation, which is the biggest obstacle to prevent people from obtaining specific drugs, and lobbying Congress to reduce the authority of FDA, but this has not affected the sacred protection and performance of its mission and responsibility. Today, FDA has become a golden shield in the hearts of global food and drug consumers. And supervise the safety of its domestic products.
"GMP" is the abbreviation of English Good Manufacturing Practice. 1969, the world health organization recommended the use of GMP to all countries in the world. In Chinese, it means "good practice" or "good manufacturing standard", which is an independent management system that pays special attention to product quality and health and safety in the production process. It is a set of mandatory standards applicable to medicine, food and other industries, and requires enterprises to meet the hygiene and quality requirements in raw materials, personnel, facilities and equipment, production technology, packaging and transportation, quality control and so on. , form a set of operating norms to help enterprises improve the sanitary environment, and find out the problems existing in the production process in time and improve them.
USP United States Pharmacopoeia (USP)- Organization Overview Introduction USP sets quality standards for prescription and over-the-counter drugs, food supplements and other health care products, and cooperates with health care institutions to help them meet the standards. Since the establishment of 185, these standards have been contributing to ensuring access to quality pharmaceutical services all over the world. USP is a recognized legal public standard-setting organization in the United States, and these reference materials have been recognized and used in more than 30 countries around the world. USP is an independent public health organization based on science. As a self-sufficient non-profit organization, USP's funds come from the sales of products and services, and its products and services are aimed at ensuring the public to obtain high-quality pharmaceutical services. With the active participation and supervision of professional volunteers, USP has made more and more contributions to the public health industry. These volunteers represent the health care industry, as well as academia, government departments, pharmaceutical industry, health planning and consumer organizations. Our mission USP establishes and promotes the quality standards and information resources of health care and related products and practices to promote public health. Our standards and information can help patients and doctors maintain and improve their health.
High-quality product quality-standards and certification USP establishes public standards to ensure the excellent quality of drugs, food supplements, health care and medical-related products. According to federal laws applicable to such standards, prescriptions and over-the-counter drugs used in the United States must meet USP standards. In order to ensure the quality of drugs and related products, many other countries also require the adoption of high quality standards, just like USP standards. USP disseminates its standards to manufacturers, pharmacists and other users through USP-NF and other publications, statutory USP standard materials and professional education courses.
USP also hosted a certification program for ingredients and products of food additives. These plans include independent tests and audits aimed at certifying the integrity, purity and specifications of ingredients and products for participating manufacturers. Patient safety USP implements two programs to provide safer care for patients who are taking medicine and being hospitalized. The drug error reporting program enables medical professionals to report drug errors directly to USP.
The Doctor's Desk Reference Manual, written by the American medical authority PDR, is an authoritative reference book recognized by the American medical community. It is compiled by pharmaceutical companies and edited by lawyers and officials. Detailed examples of prescription drugs approved by the US Food and Drug Administration (FDA) are one of the necessary materials for medical clinics, hospitals and pharmacies in the United States.
The FDA-approved drug information and related contents provided by PDR "Doctor's Desk Reference Manual" in the United States can effectively improve the safety of patients, make patients have a more official understanding of drug use for a certain disease, effectively avoid improper drug use, make patients and doctors choose effective drugs more correctly, and reduce professional medical responsibility.
The National Health Foundation (NSF), founded in 1944, is an independent non-profit NGO. NSF is committed to standard setting, product testing and certification services in the field of public health, safety and environmental protection, and is an authoritative organization in the field of public health and safety. Millions of consumer goods, commercial and industrial products are printed with NSF logo every year, which has been trusted by consumers, industry insiders and manufacturing units for many years. The purpose of NSF is to formulate and implement management plans for public health, services, research and education environment. As a reliable and neutral organization, NSF provides services to the government, industry and consumers, and solves public health and environmental problems.
NSF's technical resources include test equipment, analytical chemistry and microbiology laboratory. NSF professionals include engineers, chemists, toxicologists, public health scientists and computer scientists, who have rich experience in public health, food safety, water quality and environment. The certification issued by NSF has been recognized by American National Standards Institute (ANSI) and Canadian Standards Committee (SCC).
As a neutral third party, NSF has been recognized and certified by 13 national or industry authorities, including American National Standards Institute (ANSI), American Occupational Safety and Health Administration and Canadian National Standards Committee. NSF is the designated cooperation center of the World Health Organization (WHO) in food safety and drinking water safety and treatment. Products that have passed the NSF test and reached the NSF standard are authorized to use the NSF mark, so any product authorized to print the NSF mark means that the product has been confirmed in the following aspects:
1, which can achieve the ability of removing impurities marked in the product manual;
2. The materials that make up the product will not add pollutants to the water during the water treatment process;
3, in line with the design and production process requirements;
4. The product has no structural and functional defects;
5. The certification standards shown in product advertisements, sample materials and labels are true and accurate.
NSF certification system is of great significance to people in the industry, consumers and manufacturing units. NSF, a credible, objective and independent third-party monitoring organization recognized by the public and the government, has tested and verified that the products meet specific standards, which means that the products with the logo have undergone rigorous testing and made a guarantee to consumers. All units participating in the NSF certification system must be tested, retested and inspected/audited by a third party, and manufacturing units must follow open standards when producing products. Standards include product manufacturing standards, materials, design, process flow, etc.
At the same time, NSF requires that if a company wants to print the NSF logo on its products, it must meet the strict requirements of NSF certification and authorization. These requirements include initial and periodic testing and evaluation, and even surprise inspection. If the logo is found to be misused, or the product does not meet the requirements, NSF can seal up, seal up the products and goods in stock, even destroy the unqualified products and blacklist them, and take measures such as recall, legal action, informing the public and canceling the certification qualification. Or other harsh actions. NSF represents the interests of all parties, and will control the behaviors of insiders, consumers and manufacturing units, and supervise the implementation of policies and the authority of certification.
UNPA (United Natural Products Alliance)-American Natural Products Alliance is an organizational alliance of dietary supplements and functional food companies and natural health products, and promises to provide customers with excellent quality, efficiency and reliability.
The history of UNPA is also unique. 199 1, eight dietary supplement and health care products companies in Utah agreed to form an alliance to challenge the US FDA's infringement and improper law enforcement actions against supplement companies. At that time, the association was called Utah Natural Products Alliance.
UNPA initiated a strategy to rewrite the dietary supplement rules. The plan was worked out jointly with Senator orrin hatch's office, and passed the 1992 Health Freedom Act initiated by Senator orrin hatch and Congressman Bill Richardson of New Mexico. This bill eventually became the dietary supplement health and education law of 1994 (DSHEA). Apart from the Vietnam War, the history bill of the US Congress is uncontroversial. In 2005, the association was renamed the American Natural Products Alliance, with more diverse members, and now it spans the United States, Canada, Europe and Asia. The core task of UNPA is to help ensure the full and proper implementation of the National Defense, Security and Health Law. This includes a series of laws and regulations supporting DSHEA, such as GMP regulations, adverse event reporting system, analysis method development, steroid control as a supplement, international quality management agreement, etc.