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Congratulations! Your organization has gained regulatory approval and launched its medical device product. The ‘History’ in Design History File may elicit impressions that all those design and development requirements are now done and considered part of the past. However, several components of the DHF continue as a reference and evolve, including requirements and risk management. […]
In the competitive world of medical device development, medical device companies can’t afford to lag behind the pack. Streamlining the design and approval process is vital to getting products to market in a timely manner. Proper documentation is key to a smooth approval process. One essential ingredient to medical device documentation is the Design History […]
magniX chooses Jama Connect for its ease of use, quick deployment, and to help modernize their requirements management program and demonstrate compliance with standards. Headquartered in Everett, Washington – located just outside of Seattle – magniX is the leading developer of propulsion systems for electric aircraft, including motors, inverters, and motor controllers. magniX is working to […]
In this post, we look at non-functional requirements are tracked by agile product teams and how they impact the product development cycle. Imagine that you’re in the market for a new car. As you shop, you have a couple of non-negotiable features or attributes in mind, such as saving destinations within the car’s built-in GPS […]
In this blog post, experts from Cadence, OpsHub, and Jama Software talk about enabling digital transformation in the hardware and semiconductor industries. The relentless pace of innovation, rapidly changing markets, and increasing product complexity are creating intense pressures on companies in the semiconductor and hardware space. Some of the biggest challenges relate to scaling effectively […]
Reviews play a key role in successful product and systems development, helping to ensure the new project meets stakeholder, market, and compliance requirements. Peer and approval review processes enables organizations to both iterate and innovate quickly, while providing a dedicated process to apply appropriate rigor for final reviews. In addition, integrating item workflow with approval reviews can eliminate manual processes and […]
In January 2020, NASA reported that Model-Based System Engineering (MBSE), “has been increasingly embraced by both industry and government as a means to keep track of system complexity.” And in order to help facilitate accelerated adoption of MBSE, we’re proud to introduce Jama Connect® for Traceable MBSE™. Jama Connect for Traceable MBSE is a single […]
When we buy a new cell phone or TV or computer, do we buy-in for what it is? Of course not. We buy it for what it will do for us. Likewise, when companies or governments buy new systems or new enterprise software products, they couldn’t care less about the products themselves. What they care […]
Requirements management (RM) is a challenge for many companies, partly due to the ambiguity involved in software development. First, you must understand the client’s requirements. Second, you must match those requirements to critical processes. RM is a component of requirements engineering (RE), which bridges the divide between a client’s needs and what developers create. When […]
Over the last decade, digital health solutions have become increasingly important, powering revolutionary developments in areas such as robotics, genomics, diagnostics, patient/provider interactions, and many more. In our recent webinar with MDM Engineering Consultants and BeanStock Ventures, we talked about critical standards and best practices to follow. Attendees also heard critical insight from industry leaders […]