As a medical device manufacturer, you face pressure to reduce the time-to-market in every aspect of the product development lifecycle. Gain expert insights from the powerful partnership between Parasoft and Velentium.
Their joint focus offers organizations professional engineering consulting that specializes in medical device design and development, cybersecurity, manual-to-fully-automated test systems, and manufacturing—now supported by Parasoft’s automated software testing tool suite to ensure medical devices comply with the IEC 62304 standard and gain FDA approval.
Key takeaways:
- Learn how Velentium cuts costs and time-to-market with Parasoft’s tool suite
- Overview of the medical device secure development lifecycle
SAST and the secure coding conventions
- Theory and different types of testing for medical devices
