Medical devices represent a significant sector of the U.S. healthcare industry, with annual sales exceeding $13 billion. These devices, including pacemakers, cardiac defibrillators, infusion pumps, and neural stimulators, have unacceptably high failure rates. Missing safety requirements in the product specification are often the source of harm to patients.
For next-generation devices, which are much more complex, we must include robustness requirements in the specifications through hazard analyses during the concept stage. FDA approval hinges on demonstrated safety and the reliability of the safeguards. Including safety requirements early reduces the time to market.
Attend this webinar to learn how you can design medical devices that ensure patient safety. We will also review hazard analysis techniques and safety design techniques for devices, including next-generation ones.
For next-generation devices, which are much more complex, we must include robustness requirements in the specifications through hazard analyses during the concept stage. FDA approval hinges on demonstrated safety and the reliability of the safeguards. Including safety requirements early reduces the time to market.
Attend this webinar to learn how you can design medical devices that ensure patient safety. We will also review hazard analysis techniques and safety design techniques for devices, including next-generation ones.
