How a Smarter Risk Management Process Improves Business
Improving your risk management process means safer products. In many cases, it can also give your overall business a boost that impacts efficiency, collaboration, and innovation.
Improving your risk management process means safer products. In many cases, it can also give your overall business a boost that impacts efficiency, collaboration, and innovation.
Earlier this year, we introduced Jama Connect™ Risk Management Center for medical device developers, and now we’re excited to announce that we’re opening it up to all our customers working within regulated industries with the introduction of FMEA templates.
Prominent research and consulting firm Frost & Sullivan recently observed the product development landscape and its relationship to risk. The output is a recently-released brief, “Safeguarding Regulated Products Amidst Growing Complexity,” that spotlights Jama Connect™ as a remedy for ineffective risk analysis in product development.
“The biggest benefit for us is the efficiency in completing and gaining agreement on requirements and testing procedures.”
Compliance standards that involve relatively new functional safety elements, will likely add additional requirements to the development process.
Close gaps in product development with Jama Connect™ and LDRA Interested in closing gaps in your product development lifecycle? It’s no secret that developers of mission-critical software are facing increasingly complex system requirements and stringent standards for safety and efficacy. That’s why Jama Software has partnered with LDRA to deliver a test validation and verification […]
Here are the top three ways that products have become more complicated in the last five years, according to a recent study done by engineering.com.
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.
With more public attention than ever being paid to the fast-moving, competitive, lucrative and sometimes life-changing world of medical device development, it sounds obvious to say that no company wants to experience a product recall.
Despite a common misconception, Agile is compatible with all industries – even those with strict regulatory standards.
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