Other content in this Stream
Read the story about how a leading dental company switched from a document-driven requirements management process to a more modern approach with Jama Connect.
Medical device companies must evaluate how their development process stands up to the challenge of increasingly connected technologies and strict regulation.
You’ll gain more confidence that your recently-released products avoid recalls, fines, or worse if you perform failure mode and effects analysis (FMEA) as part of your risk management.
1:06:09Failure Modes and Effects Analysis (FMEA) is a common and trusted risk assessment tool used by systems and product development teams to manage risk early.
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
RBC Medical Innovations selects Jama Software’s modern requirements management solution, Jama Connect, to help unify processes and enhance traceability for medical devices.
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.
Developing complex systems and products requires teams to have the ability to effectively define and track requirements, adhere to safety-critical regulations, collaborate and communicate...
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...
Read this datasheet to find out how to manage both risks and requirements directly within Jama Connect.
Tips for Medical Device Companies, Interested in Risk Techniques following ISO 14971, ISO 13485, FMEA, FTA, and 21 CFR Part 820.
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...
Last week, Jama Software launched Jama Connect Risk Management Center, which helps teams speed time-to-market without compromising quality or compliance. In our experience working with more...
Prominent consultancy group Frost & Sullivan describes how Jama Connect can help businesses thrive in safety-critical product markets.
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...
With Jama Connect™, Risk Management Center, and Medical Device Services, cross-functional medical device teams can innovate more efficiently while ensuring compliance with FDA and ISO regulations.
We are excited to announce we have extended the scope of our certification from TÜV SÜD to include medical device and railway application development.
After extensive industry research and interviews with customers in the medical device space, Jama saw an opportunity to provide a more straightforward, intuitive approach based on industry best...
With the growing amount of connected medical devices, the number of potential targets for hackers and other cyber criminals to exploit continues to rise.