What are the regulations regarding the promotion and advertising of drugs?

In New York, pharmaceutical companies must follow certain regulations when it comes to the promotion and advertising of drugs. These regulations are in place to protect the public from false or misleading information. Under New York law, pharmaceutical companies must include all risk information on promotional materials. This includes potential side effects, hazards, and contraindications associated with the drug. The promotional materials should also include the potential uses of the drug, as well as the intended patient population. Additionally, pharmaceutical companies must include a statement that the drug is intended to be used as part of a medical regimen prescribed by a healthcare professional. Another regulation is that pharmaceutical companies must keep promotional materials within approved labeling which can be found on the Drug Facts label. The Drug Facts label is a product label required by the FDA that includes basic information about the drug, such as active ingredients, inactive ingredients, indications for use, and directions for use. Lastly, pharmaceutical companies must provide evidence of a drug’s efficacy through randomized clinical trials and other scientific data. Promotional materials should also include disclaimers that the drug is not intended to treat any medical condition, or to be used as a cure or preventative measure. Such disclaimers should be clearly and prominently displayed. By following these regulations, the public can be assured that they are receiving accurate information regarding the safety and efficacy of drugs.

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What are the regulations regarding the promotion and advertising of drugs?

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