What is FDA Certification?
Release time:
2021-12-08
FDA is the United States Food and Drug Administration (U.S. Food and Drug Administration), it is the international medical audit authority, authorized by the United States Congress, the federal government, specializing in food and drug management of the highest law enforcement agencies. The FDA is a government health regulatory body composed of doctors, lawyers, microbiologists, pharmacologists, chemists, and statisticians dedicated to protecting, promoting, and enhancing the health of the nation. FDA-certified foods, drugs, cosmetics and medical devices are safe and effective for the human body. In nearly 100 countries such as the United States, only materials, devices and technologies approved by FDA can be commercialized for clinical application. Most of the federal laws enforced by the FDA are codified in the Federal Food,Drug,and Cosmetic Act, also known as Title 21 of the United States Code. Other laws entrusted to the agency for enforcement include the Public Health Service Act (the Public Service Act), the Substance Misuse Management Act (the Controlled Substances Act), the Federal Anti-Tampering Act (the Federal Anti-Tampering Act), and the Family Smoking Prevention and Tobacco Control Act. The U.S. Food and Drug Administration has a wide range of safety regulations. For example, the regulation of prescription drugs involves every aspect of it, from drug testing, manufacturing, labeling, advertising, marketing, utility to drug safety. Regulation of cosmetics is limited to labeling specifications and safety. The agency's regulatory actions for most products are based on a series of publicly available standards, supplemented by a certain number of instrument checks.
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