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.
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.
Klockner Pentaplast (Gordonsville, VA) offers a version of calendered Barex® film from BP Chemicals with high oxygen barrier properties. Applications include food, medical device and chemically resistant packages.
The Sterilization Packaging Manufacturers Council (SPMC) of the Flexible Packaging Association (FPA) is revising current standards and identifying areas where standard test methods are needed for flexible packaging intended for medical use.
Scimed Life Systems uses up its $250ꯠ preprinted label stock inventory in favor of on-demand high-quality four-color process thermal-transfer printing. Label stock changeover drops from 20 per shift to just over one.
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.