WHITE PAPER -
Producing high-quality, feature-rich software while meeting regulatory guidelines presents a unique set of challenges for those developing medical device software. The key to success is implementing an effective software verification process that maximizes development productivity and best practices while ensuring code quality and security.
Posted: February 22, 2010 | Published: November 1, 2009
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Embedded software development teams in the medical device sector are striving to meet growing market demands while dealing with increased software complexity across global teams, business and engineering challenges with limited engineering resources and increased code complexity. Read this paper to learn how to optimize productivity challenges.
Posted: February 22, 2010 | Published: July 1, 2009
WHITE PAPER -
As Agile is embraced by development organizations everywhere, the need to produce clean, maintainable software quickly is great. To achieve development agility, developers must maintain velocity, eliminate bug debt, and focus on peer interaction. Read this paper to learn how to automate time consuming development activities to boost productivity.
Posted: February 22, 2010 | Published: November 1, 2009
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Software development teams aiming to achieve DO-178B certification can streamline their efforts with source code analysis tools. In this white paper, learn how the defect, architecture, and metrics analysis capabilities of Klocwork source code analysis can be used to automate time consuming tasks and achieve key objectives of the DO-178B guidance.
Posted: February 22, 2010 | Published: March 1, 2009
WHITE PAPER -
Producing high-quality, feature-rich software while meeting regulatory guidelines presents a unique set of challenges for those developing medical device software. The key to success is implementing an effective software verification process that maximizes development productivity and best practices while ensuring code quality and security.
