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Sagot :
Answer:
True
Explanation:
The FDA guidance requires pharmaceutical companies to present both benefit and risk information when promoting their FDA-regulated products on social media. ... Such information needs to be provided regardless of any character space constraints on some social media platforms such as Twitter.
True, the FDA cannot control the content of celebrity Tweets on prescription drugs.
What is FDA?
Located under the Department of Health and Human Services, the Food and Drug Administration (FDA or USFDA) is a federal organization. The FDA is in charge of ensuring the safety of food, tobacco products, dietary supplements, prescription and over-the-counter medications, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed, and veterinary products in order to protect and advance public health. The Federal Food, Drug, and Cosmetic Act (FD&C) is the FDA's major area of enforcement, although the organization also upholds related regulations and other laws, most notably Section 361 of the Public Health Service Act. A large portion of this regulatory-enforcement job concerns the regulation of condoms, lasers, cell phones, and other items, as well as the prevention and control of disease in settings ranging from domestic pets to donated human sperm for assisted reproduction.
Depending on the kind of product, any potential risks, and the agency's regulatory authority, many safety regulation schemes exist. For instance, the FDA controls practically every aspect of prescription pharmaceuticals, including testing, manufacturing, labelling, advertising, marketing, efficacy, and safety; meanwhile, the FDA primarily controls labelling and safety for cosmetics. With a set of stated standards and a sparse number of facility inspections, the FDA monitors the majority of products. On Form 483, inspection observations are recorded.
A number of laws passed by the US Congress and interpreted by the FDA control how the Food and Drug Administration regulates foods and dietary supplements. The Federal Food, Drug, and Cosmetic Act and related laws give the FDA the power to regulate the quality of substances sold as food in the US and to keep an eye on any claims made on food labels regarding their composition or health benefits.
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