The U.S. Food & Drug Administration (FDA) is reviewing its labeling requirements for drugs, medical devices and biologics to ensure that health practitioners and patients are provided with what the agency believes is more thorough than what's currently provided.
Environmental regulation of packaging has become a hot item outside the U.S. this year. More than 20 countries worldwide now have some form of "producer responsibility" law on the books or in the works.
Special thermoformed packaging for a medical device from Medex of Dublin, OH, is designed so that clinicians in a non-sterile environment can open the package and present its contents to surgical staff in a sterile operating room without compromising the product's sterility.
At a time when most surgical glove pouches consist of paper webs that are cold-sealed together, ECI Medical Technologies is positioning its product at the high end by introducing gloves in a clear film pouch that's printed gravure in two colors.
June 30, 1996
Critics of the U.S. Food and Drug Administraton (FDA) frequently cite the agency's snail-like pace in approving everything from new drugs and medical devices to food additives (including direct-contact food packaging) and health and nutrient content claims on food labels.