What is a major responsibility of the FDA regarding health products?

The major responsibility of the FDA, or the Food and Drug Administration, is to guarantee the quality and safety of drugs and medical devices. This involves rigorous evaluation processes, including clinical trials and scientific assessments, to ensure that health products are effective for their intended use and do not pose unreasonable risks to patients.

The FDA's role is critical in maintaining public health standards, as it sets forth regulations that manufacturers must adhere to before a product can be released to the market. This includes reviewing data on a product's safety, efficacy, and manufacturing practices. By ensuring that products meet these standards, the FDA helps protect consumers from potentially harmful or ineffective medications and devices, ultimately supporting a safer healthcare system.

The other options, while related to health and pharmaceuticals, do not accurately describe the core responsibilities of the FDA. For instance, introducing new drugs to the market involves a rigorous review process rather than a responsibility of simply introducing them. Similarly, the FDA does not regulate the pricing of medications, which falls under different regulatory frameworks. While promoting health education among the public is important, it is not a primary responsibility of the FDA compared to ensuring the safety and quality of products.