Industry economics and related laws of Dietary Supplement
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Industry economics and related laws of Dietary Supplement

Views: 0     Author: Site Editor     Publish Time: 2022-06-27      Origin: Site

Industry economics and related laws of Dietary Supplement

With the rapid development of China's health food industry, the management of its raw materials and products needs to be continuously improved to meet the growing needs of the people for a better life. The United States has the largest health food market in the world, which provides material for health food researchers and regulation-making departments in China to draw on. So, let's take a look at the industrial economy and related laws regarding Dietary Supplement in the United States. Here are some answers.


Here is the content list:

l The Dietary Supplement industry is an important part of the US economy.

l Laws relating to the Dietary Supplement in the US.


The Dietary Supplement industry is an important part of the US economy.


The Dietary Supplement industry is an integral part of the US economy and the industry has always been committed to a positive trade balance. It is estimated that 600 Dietary Supplement manufacturers in the United States produce approximately 4,000 products, with annual sales of at least $4 billion for these products alone. To promote health, the US government has taken legislative action to protect consumers' rights to safe Dietary Supplements and to establish a rational federal framework to replace the ad hoc patchwork of Hard capsules regulatory policies, thus amending the Federal Food, Drug, and Cosmetic Act and creating the Dietary Supplement Health and Education Act (DSHEA). The DSHEA was an important milestone in the regulation of the Dietary Supplement in the US.


Laws relating to the Dietary Supplement in the US.


In addition to the FD&C Act and DSHEA, the Nutrition Facts Labeling and Education Act of 1990, an amendment to the FD&C Act, requires that most foods must have a nutrition facts label and that the food label posted must contain a statement of nutrient content, as well as some health information to meet specific requirements. The Dietary Supplement Good Manufacturing, Packaging, Labelling and Storage Practices (CGMP), issued in 2007, covers the requirements for personnel, premises, equipment and facilities, production and process control systems (quality control, package labeling, manufacturing records, batch production records, laboratory operations, manufacturing operations, packaging and labeling operations), storage and transport, repatriation of the Immunity increases, product complaints, records, and documentation. The Food Safety Modernization Act (FSMA) of 2011 amended the FD&C Act concerning the safety aspects of the food supply, with an emphasis on improving prevention, monitoring, and response to food safety issues. The Food Safety Modernisation Act 2011 (FSMA) amends the FD&C Act regarding the safety aspects of the food supply, to improve the prevention, monitoring, and response to food safety issues so that the industry and consumers can better understand and implement the Act. Draft Guidance Document New Dietary Supplement Declarations and Related Issues, food Labelling Guidelines.


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