There are many theories on how to write better requirements. Some suggest using or excluding certain words or limiting each requirement to one sentence. However, there’s a danger in having too many rules around your requirement writing process because it can end up hamstringing your work. Writing excellent requirements, in my opinion, is both an […]
A requirements, risk, and test management platform that centralizes everything into one system of record can provide the single source of truth missing from many product development processes.
Being a former McKinsey consultant, I have spent too much time immersed in frameworks, maturity models and methodologies. As I age, and my pragmatism grows, I find that many maturity models are too high level and vague and do not reflect the actual progression companies go through as they mature a given business function. What I do find extremely useful are empirical maturity models since they categorize what companies are ACTUALLY doing TODAY in response to given challenges and pressures. Unfortunately, […]
In this post, we discuss how as product development processes become more complex, traditional document-based requirements management shows its limitations.
While writing requirements is both an art and a science that will vary by context, here are five best practices for writing crystal clear requirements.
EDITOR’S NOTE: This post on requirements was originally published here, by Medium, and this article was adapted from Software Requirements, Third Edition, by Karl Wiegers and Joy Beatty. If you’re interested in software requirements management, business analysis, project management, software quality, or consulting, Process Impact provides numerous useful publications, downloads, and other resources. Creating a Culture that […]
WEBINAR: TIR45 | An AGILE Approach to Software Regulatory Compliance Are you ready to seamlessly move from CLIA, Research Use Only (RUO) or Emergency Use Authorization (EUA) to a clinical software product? Join us as we discuss an AGILE approach to software regulatory compliance. We’ll be hosting this informative panel discussion with the owner of […]
Companies rely on Jama Software to align remote engineering teams and keep everybody on the same page. We can help your teams adjust to remote work, too.
Get a recap of our popular webinar on best practices for writing requirements, and head over to our resources center to watch it now.
3 improvement strategies to insert risk control as a crucial part of the medical device development framework to comply with ISO standards and EU MDR.
USA
135 SW Taylor Suite 200
Portland, Oregon, 97204
EUROPE
Amsterdam Queens Tower
Delflandlaan 1, 1062EA Amsterdam
The Netherlands
© 2025 Jama Software