EPA and FDA Involving Risk Assessment

Federal Agencies/Acts Involving Risk Assessment Paper
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The Environmental Protection Agency (EPA) and the Food and Drug Administration (FDA) play an instrumental role in the United States carrying out risk assessments concerning substances, chemicals, and products across different areas, including consumer goods, environmental health, and workplace safety. This paper critically compares EPA and FDA, discussing their mandates, responsibilities, processes, risk management, and communication strategies. By evaluating the similarities and differences between the two federal agencies, the paper seeks to establish valuable insights into their specific roles and the approaches they incorporate to ensure environmental well-being and public health.
Mandates and Responsibilities
The EPA's primary obligation is to safeguard public health and the environment. Its responsibilities primarily lie in conducting risk assessments regarding environmental pollutants, chemicals in industrial processes, and hazardous substances. It evaluates the effect of such pollutants on ecosystems, water, air, and soil. On the other hand, the FDA is mandated to enhance food and cosmetics' efficacy