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A group of researchers representing devicemakers, academic institutions and the FDA has published a list of factors device developers should consider when collecting patient preference information (PPI) to help design trials. Read More
A Rhode Island state jury has awarded $4.8 million in damages against Becton Dickinson for alleged injuries caused by its Ventralex surgical hernia repair mesh product. Read More
Philips Respironics is voluntarily recalling certain sleep therapy masks due to concerns that their magnetic headgear clips or straps could adversely impact metallic implanted devices or other metallic objects inside the body. Read More
Excellus Holdings, San Diego, Calif., has drawn an FDA Form 483 for inspectional observations that include senior management passing the buck on customer complaints. Read More