Medical devices are nowadaysmore and more software dependent, and software malfunctioning can lead to injuries or death for patients. Several standards have been proposed for the development and the validation of medical devices, but they establish general guidelines on the use of common software engineering activities without any indication regarding methods and techniques to assure safety and reliability. This paper takes advantage of the Hemodialysis machine case study to present a formal development process supporting most of the engineering activities required by the standards, and provides rigorous approaches for system validation and verification. The process is based on the Abstract State Machine formal method and its model refineme...
Software as a medical device is subject to dedicated regulatory requirements before it can be used o...
In the last decade, the use of information technology (IT) in healthcare has taken a growing role. I...
Embedded software in medical devices is increasing in content and complexity. Traditional software v...
Medical devices are safety-critical systems since their malfunctions can seriously compromise human ...
Medical device software malfunctioning can lead to injuries or death for humans and, therefore, its ...
The development of medical devices is a safety-critical process, because a failure or a malfunction ...
The use of formal methods is often recommended to guarantee the provision of necessary ser-vices and...
Software controlling medical devices is safety-critical since human safety depends upon its correct ...
Safety-critical medical devices play an important role in improving patients health and lifestyle. F...
The benefits of effective verification and validation activities in the medical device domain includ...
The paper describes the practical use of a model checking technique to contribute to the risk analys...
The paper is concerned with the practical use of formal techniques to contribute to the risk analysi...
International audienceFormal methods have emerged as an alternative approach to ensuring quality and...
The paper is concerned with the practical use of formal techniques to contribute to the risk analysi...
We present a formal specification and analysis of a haemodialysis machine (HD machine) in Event-B us...
Software as a medical device is subject to dedicated regulatory requirements before it can be used o...
In the last decade, the use of information technology (IT) in healthcare has taken a growing role. I...
Embedded software in medical devices is increasing in content and complexity. Traditional software v...
Medical devices are safety-critical systems since their malfunctions can seriously compromise human ...
Medical device software malfunctioning can lead to injuries or death for humans and, therefore, its ...
The development of medical devices is a safety-critical process, because a failure or a malfunction ...
The use of formal methods is often recommended to guarantee the provision of necessary ser-vices and...
Software controlling medical devices is safety-critical since human safety depends upon its correct ...
Safety-critical medical devices play an important role in improving patients health and lifestyle. F...
The benefits of effective verification and validation activities in the medical device domain includ...
The paper describes the practical use of a model checking technique to contribute to the risk analys...
The paper is concerned with the practical use of formal techniques to contribute to the risk analysi...
International audienceFormal methods have emerged as an alternative approach to ensuring quality and...
The paper is concerned with the practical use of formal techniques to contribute to the risk analysi...
We present a formal specification and analysis of a haemodialysis machine (HD machine) in Event-B us...
Software as a medical device is subject to dedicated regulatory requirements before it can be used o...
In the last decade, the use of information technology (IT) in healthcare has taken a growing role. I...
Embedded software in medical devices is increasing in content and complexity. Traditional software v...