Which government agency is responsible for setting standards for the control of drugs?

The Food and Drug Administration (FDA) is the government agency responsible for setting standards for the control of drugs in the United States. The FDA’s mission encompasses the regulation of drugs, ensuring their safety, efficacy, and security. This involves reviewing new drug applications, monitoring ongoing clinical trials, and ensuring that pharmaceutical manufacturing practices meet established guidelines. Through these regulations, the FDA plays a crucial role in public health by controlling what is available to patients and ensuring that consumers have access to safe and effective medications.

Other agencies mentioned have different focuses. The Centers for Disease Control and Prevention (CDC) primarily deals with public health issues, disease prevention, and health promotion, but does not set drug control standards. The National Institute on Drug Abuse (NIDA) is focused specifically on research and education about drugs and their effects on health, but it does not regulate drug approval or standards. The World Health Organization (WHO) operates on an international level to promote global health but does not set national drug regulations. Each has its important role in public health and drug-related matters, but the FDA is the key agency for the regulation and control of drugs within the U.S.