FDA: Public health and safety is our top priority

The modern market is overflowing with an abundance of various goods and services, and the aesthetic medicine industry is no exception. With such an influx of products and medicines, a clear, constant control over their quality is necessary, which is carried out by special organizations.

Their main goal is to prevent goods that can be dangerous to human health and life from entering the market. The standard of such a state structure is considered by the FDA – agency of the US Department of Health, read more about it on estet-portal.com in this article.

Key features of food and drug control in the United States

FDA (Food and Drug Administration) – is the US Food and Drug Administration. The authority of this department is undeniable throughout the world.

Any aesthetic medicine specialist knows that if a product or medical device is approved by the FDA, then there is no doubt about its highest quality.

This organization controls the quality of food, medicines and cosmetics, medical equipment, tobacco products. It is important to emphasize that this department also monitors compliance with all laws and standards in this area.

History of Quality Control in the United States

The organization was created in 1906 under the name of the Bureau of Chemistry. The FDA's food and drug control activities began with the passage of the "Pure Food and Drugs Act"; – Purity of Foods and Medicines Act, which prohibited the sale of falsified products or goods of poor quality. In 1931, the name of the agency was changed to the current Food and Drug Administration.

As for the head of this department, since the FDA is a government organization, he is nominated by the President of the United States and approved by the Senate.

Main Functions of the FDA Quality Assurance Organization

The Food and Drug Administration is responsible for protecting public health by ensuring the efficacy and safety of medicines, biological products, and medical devices.

Also FDA:

• ensures food and drug safety;
• is responsible for regulating the production and sale of tobacco products;
• is responsible for advancing public health by helping to accelerate innovations that make medical products more effective, safer and more affordable.

The main task of the FDA – it is to ensure the health and safety of the population.

The future of product and drug quality control

In an era when health care costs are rising at a tremendous pace, product quality requirements are becoming stricter and stricter.

Large-scale randomized clinical trials are critical in demonstrating the safety and efficacy of drugs.

However, many scientists argue that current research only determines whether one treatment is better than another. Therefore, for many specialists, the future – this is personalized medicine, which certainly requires a much more rigorous approach.

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