Smoke Detector Litigation

Smoke detectors are invaluable in saving lives. It is estimated that three-fifths of all deaths from home fires occurred in homes without smoke detectors. But what happens when a smoke detector fails to alert residents of the presence of smoke? Who is responsible for smoke detector failure?

Use of Investigational Drugs in Human Clinical Studies

In a clinical study, human volunteers receive investigational drug therapy. The effects of the treatment are compared with a control group of human volunteers who receive either the standard treatment or a placebo (a sugar pill that has no therapeutic benefit). Researchers are able to conclude whether the experimental drug had a better outcome than the standard treatment. The experimental drug might produce a better outcome, but it might not work. It could prove dangerous or even deadly.

Nurses' Liability in Administering Prescription Drugs

Drugs can be very harmful if misused. Only a licensed practitioner (physician, osteopath, nurse practitioner, or other licensed healthcare provider) can order prescription medication. Licensed nurses are permitted to administer medication to patients under medical supervision. A nurse cannot give medication to a patient without a physician's order. This article discusses a nurse's responsibility and liability in administering prescription drugs.

Common Elements of Products Liability Cases

Products liability law covers personal injury and property damage that occurs when a defective product is used. There are several elements that are common to products liability cases. First, an injured person must prove that the product was defective or harmful. Second, it is necessary to show that the product was defective when it was purchased or delivered. Third, the injured person must show that the defective product caused the injury or accident.

The FDA Modernization Act of 1997

In 1997, Congress passed legislation amending the Federal Food, Drug, and Cosmetic Act relating to the regulation of food, drugs, devices, and biological products. The new legislation, called the Food and Drug Administration Modernization Act, reduces the approval time for drugs and medical devices while maintaining patient safety. In addition, the Modernization Act provides the U.S. Food and Drug Administration (FDA) with additional resources to devote to expediting the drug and medical device review process.