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Topic: Compliance

GDPR – A Lesson in Modernization

By Bjorn Gullberg on July 25, 2017

In my profession, I meet lots of customers who are starting or in the middle of their digital transformation, and many of whom are trying to solve...

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The C/C++test, Jtest, dotTEST 10.3.2 and Development Testing Platform 5.3.2 Release

By Mark Lambert on June 20, 2017

With this week’s release of Parasoft C/C++test, Jtest, dotTEST 10.3.2, and Parasoft DTP 5.3.2, we are providing numerous enhancements to improve...

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The Cure for Software Defects and Vulnerabilities in Medical Devices

By Alan Zeichick on October 6, 2016

Modern medical devices increasingly leverage microprocessors and embedded software, as well as sophisticated communications connections, for...

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How an Engineering Approach to Automotive Software Quality Puts the Brakes on Defects

By Alan Zeichick on September 22, 2016

By Alan Zeichick (Principal Analyst at Camden Associates) and Arthur Hicken, Chief Evangelist at Parasoft  Cars are more complex than ever, and...

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How a Medical Device Co. Cut Testing Costs in Half

By Parasoft on August 6, 2015

Bovie Medical Corp. is a leading maker of medical devices and supplies as well as the developer of J-Plasma®, a patented new plasma-based surgical...

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How to Leverage Automotive Software Development Standards to Mitigate Risk

By Parasoft on July 9, 2015

Some organizations view compliance with ISO 26262, MISRA, and other standards as an overhead-boosting burden, but the truth is that the cost of...

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How Static Analysis Reduces the Burden of Pharmaceutical Industry Regulatory Compliance

By Parasoft on January 19, 2012

Since 1961, IMA has been designing and producing implants and equipment for packaging in the food and pharmaceutical industries. By adopting...

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Static Analysis for FDA: 3 Keys to Success

By Parasoft on June 23, 2011

Continuing our series of posts on static code analysis for FDA/medical device sofware compliance

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Static Analysis for FDA: What's Involved?

By Parasoft on June 16, 2011

In last week's post, we introduced how static analysis is just one piece of the FDA compliance puzzle. In the next posts, we'll explore this...

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