Author Bio
No one sets out to create a product that’s an abject failure, which is one of the reasons Failure Mode and Effects Analysis (FMEA) exists.
Skipping the requirements doc really isn’t a viable approach. How, then, can you create a good product requirements document with minimal hassle?
What better reference point for collaborative engineering than the most famous songwriting duo of all time: The Beatles’ John Lennon and Paul McCartney.
While connected medical devices provide opportunities for instantaneous results and early intervention, they’re also more vulnerable to cyberattacks.
This month, as individuals, organizations, businesses, and allies, we came together to honor, celebrate, and show support for the LGBTQ+ community.
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.
Adopting these four best practices around modern requirements management and requirements traceability will help your team ensure product quality, decrease time-to-market, and achieve regulatory compliance.
To help Jama’s avionics customers develop safe, quality products on expedited timelines, we’ve teamed up with the safety-critical experts at AFuzion.