What is the legal framework for drug safety?

Drug safety is a crucial element of health care law in Pennsylvania. Federal and state governments work together to ensure that drugs are properly monitored for safety and effectiveness. At the federal level, the U.S. Food and Drug Administration (FDA) is responsible for controlling the safety and effectiveness of drugs in the United States. The FDA evaluates the safety of drugs through a rigorous approval process and regulates manufacturing standards to guarantee the quality of drugs. In addition, the FDA also ensures that the labeling and packaging of drugs is accurate and up-to-date. At the state level, the Pennsylvania Department of Health (DOH) is responsible for monitoring the safety of drugs in the state. The DOH ensures that drugs are stored, labeled, and administered correctly in healthcare facilities and pharmacies throughout the state. The DOH also inspects healthcare facilities to determine compliance with state and federal laws. Finally, the Pennsylvania Board of Pharmacy (PBP) is responsible for regulating the sale and distribution of drugs in the state. The PBP ensures that pharmacists properly dispense drugs and adhere to the standards set by the FDA and DOH. The PBP also reviews and updates drug labels to ensure accuracy and ensure that healthcare providers are educated about the risks and benefits of drugs. Through the combined efforts of these organizations, Pennsylvania is able to ensure proper drug safety and protect the health of its citizens.

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What is the legal framework for drug safety?

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