Sharing more information with design partners on device function and its inherent risks can help guide better decisions during the product development process, and keep patients safer.
These three practical methods can help facilitate success.
Experts at hospitals state that they need clearer and more organized information from device manufacturers during a recall.
Industry experts share advice that could influence company success.
CDRH’s Carl Fischer shares the agency’s approach to organizing and managing complaints.
We all talk about cross-collaboration, but do we really practice it?
Following these strategies will change how your company works with its outsourcing partners.
Discussing device problems can have a serious affect on patients. Physicians, manufacturers, and FDA should clarify their message to maintain trust.