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Approximately 400,000 hospitalized patients each year experience some type of preventable harm related to medical devices. The cause could be medical equipment flaws, design mishandling or user error malfunctions – all of which can be prevented with a robust usability engineering plan.
A recent report from Forrester Research, “Now Tech: Agile Requirements Management Tools, Q2 2018,” outlines the state of the market for Agile RM solutions and lays out the questions customers should ask when selecting the right requirements solution for their space.
Whether you’re just entering the automotive market or looking to improve your development process, you’ll need to become extremely familiar with the ISO 26262 standard. There are plenty of updates to sort through in the ISO 26262 2018 version, from building motorcycles to providing more guidance for the semiconductor industry.
Ease the pain of managing complex product development by connecting Jama Connect and Jira Software.
Explore how proper data collection and analysis can make your product development process more predictable.
Here are three ways to take your development process to the next level and decrease costly overruns for good.
With Jama’s Test Management Center, Quality Assurance (QA) teams can design reliable testing strategies resulting in defect-free products that adhere to even the strictest compliance standards.
Tektronix knew that with an upcoming launch, a single error in the design of an oscilloscope could lead customers to catastrophic failure. That’s why they switched to Jama.
When building complex products that must adhere to strict standards, too often the functional safety team gets looped in after development has begun.
Whether you’re an established medical device company or a new player, every stakeholder faces numerous challenges to keep up with the pace of the market while delivering compliant products that ensure patient safety.