The FDA approval process for regulated products is as diverse as the product itself. These differences are determined by applicable statute by the FDA and the relative risk of the product to the consumer. The FDA aims to provide consumers with safe and effective products.
From product testing to label inspection, the FDA tests nearly every aspect of food and medicine to ensure that they are "safe and effective" for use. You can browse the web to know the directory of FDA standard drugs.
It may not have occurred to you that most of the products you use throughout the day are regulated by the FDA. You can pick up a juice label for breakfast, the cosmetics you put on your latest hair dye, or the pain relievers you take are all FDA approved.
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With FDA approved products, you can rest assured that you won't be fooled by counterfeit ingredients on product labels. The FDA approval process ensures that the ingredients under test are used in the manufacture of goods, be they pharmaceuticals, cosmetics, or food products.
The FDA motto is to ensure the safety and satisfaction of consumers with the medicines and daily foods they consume. However, the FDA has a strict mission and the following four roles under the Food and Drug Administration Act:
* Promotes wellness through research reviews and new product approvals.
* To ensure that food and pharmaceuticals are labeled safely and correctly.
* Work with other countries to "reduce regulatory burdens".
* Work with experts and users to complete this task effectively.