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Quality system lapses — including process validation snafus — failure to address nonconforming products and not evaluating suppliers efficiently are some of the reasons contract device manufacturer Troy Innovative Instruments has fallen afoul of the FDA. Read More
Medical devicemakers soon could have a new way to measure quality, thanks to a program created jointly by the FDA and Xavier Health and recently adopted by the Medical Device Innovation Consortium. Read More
Speaking at the AdvaMed 2015 conference in San Diego, Calif., in October, an FDA representative and champion of the International Medical Device Regulators Forum Medical Device Single Audit Program renewed her call for participants in a pilot for the initiative, as companies have proven reluctant to join. Read More
For devicemakers concerned about complying with the 2013 final rule on combination products, one quality systems expert has this advice: Don’t panic. Read More
What are the barriers holding stakeholders back from having a shared view of risk? That question was at the heart of discussions held during a summit co-convened last week by the Association for the Advancement of Medical Instrumentation and the FDA. Read More
Russia’s device authority is taking a strong stance against counterfeit and unregistered products, according to representatives at separate events this month. Read More
Olympus America, Fujifilm Medical Systems and Pentax’s Hoya unit have 30 days to submit postmarket surveillance studies to the FDA detailing how their duodenoscopes are reprocessed in healthcare facilities. Read More
The International Medical Device Regulators Forum has unveiled a document it hopes will help industry understand how quality management can play a role in ensuring the quality and safety of devices that rely on software. Read More