Formal methods provide a rigorous mathematical foundation for the specification, development and verification of medical device software. This approach enhances both reliability and safety, which are ...

Laboratory-based design verification testing (DVT) of combination products and medical devices must be performed to demonstrate that the device meets the performance requirements that were set in the ...

In the medical device industry, usability plays a critical role in ensuring the safety and effectiveness of highly complex medical products. The IEC 62366-1:2015 standard, which focuses on the ...

Medical device design and development is a process that helps to ensure devices that go to market are safe, effective, marketable, and profitable. The process is a blueprint of the phases needed to ...

This course covers the systematic design of real-time digital systems and verification techniques using field-programmable gate arrays (FPGAs). The course presents a top-down design methodology, where ...

Functional safety has been a long-standing requirement for many electronics applications, including implanted medical devices, space-borne systems, and nuclear power plants. The widespread use of ...

How does EMI differ from RMI? What types of EMI and EMC affect medical devices? Shielding options. Dealing with computed-tomography interference. The medical circumstance for many people requires that ...

With the increasing size and complexity of FPGA devices, there is a need for more efficient verification methods. Timing simulation can be the most revealing verification method; however, it is often ...