Solve the Challenges of Compliance, Quality and Cost in Software Development for Medical Devices
Software is fast becoming the differentiator for manufacturers of medical devices. The rewards available from software innovation are balanced by the risks and challenges of FDA regulation, stringent quality requirements, market pressures, and significant complexity. Balancing these competing interests requires tailored application lifecycle management that addresses the unique needs of medical devices companies. This video of the MKS Solution for Medical Devices demonstrates the role that MKS Integrity can play in overcoming these challenges, by providing an application lifecycle management (ALM) platform for embedded software engineering, that streamlines FDA compliance efforts, reducing the effort required from person-weeks to mouse-clicks, while improving software quality and cycle time.
Video sponsored by MKS – Intelligent Application Lifecycle Management