Drug Supervisory Body

Target entity: Drug Supervisory Body
Context triple: [League of Nations drug control agreements, monitoredBy, Drug Supervisory Body]

• A. Health Sciences Authority
  The Health Sciences Authority is Singapore’s national regulator for health products and a key agency overseeing blood services, forensic medicine, and related public health and safety functions.
• B. Food and Drug Administration
  The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.
• C. Centre for Drug Safety
  The Centre for Drug Safety is a specialized unit within the Norwegian Institute of Public Health that focuses on monitoring, researching, and improving the safe use of medicines.
• D. Center for Drug Evaluation and Research
  The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
• E. Committee for Proprietary Medicinal Products
  The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
• F. None of above. chosen
• G. Unsure - the case is ambiguous/there is not enough information to decide.

Target entity: Drug Supervisory Body
Target entity description: The Drug Supervisory Body was an international oversight organization established under the League of Nations to monitor and regulate the global trade and production of narcotic drugs.

• A. Health Sciences Authority
  The Health Sciences Authority is Singapore’s national regulator for health products and a key agency overseeing blood services, forensic medicine, and related public health and safety functions.
• B. Food and Drug Administration
  The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.
• C. Centre for Drug Safety
  The Centre for Drug Safety is a specialized unit within the Norwegian Institute of Public Health that focuses on monitoring, researching, and improving the safe use of medicines.
• D. Center for Drug Evaluation and Research
  The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
• E. Committee for Proprietary Medicinal Products
  The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
• F. None of above. chosen