What laws and regulations apply to defective drug injury claims?

In Delaware, there are several laws and regulations that apply to defective drug injury claims. First, the Delaware Code outlines warranties that drug makers are legally obligated to adhere to when selling and marketing their products. These warranties state that the drug maker should provide customers with a safe and effective product. The Delaware Code also states that if a drug maker fails to meet one or more of these legally-binding warranties, the person who was injured by the defective drug may be able to recover damages from the drug maker. The Delaware Supreme Court has also established basic standards of proof that must be met in order for a defective drug injury claim to be successful. These standards include proving that the drug maker was negligent in its manufacturing, design, or labeling of the product. Additionally, the injured person must show that the defect caused an injury. In addition to these laws, the Delaware Department of Health and Social Services oversees the manufacturing and testing of drugs to ensure that they meet safety standards. The department also investigates reports of defective drugs and may impose fines or other penalties on drug makers who violate safety regulations. Finally, federal laws such as the Federal Food, Drug, and Cosmetic Act also apply to defective drug injury claims. This act requires drug manufacturers to ensure that their products are safe, effective, and properly labeled. If a drug maker fails to meet these standards, injured individuals may be able to pursue legal action against them.

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What laws and regulations apply to defective drug injury claims?

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