Author Bio
To meet quality demands in complex product development and improve speed to market, development teams are focusing on improving one of the most vital steps in their process: requirements management.
Thoughts on the decade ahead from Josh Turpen, Chief Product Officer at Jama Software, who oversees the ongoing innovation and refinement of our core product offerings.
When teams aren’t set up with the right tools, implementation strategies, and best practices, compliance with ISO 26262 becomes an afterthought — and an auditing nightmare.
Today’s move-fast-get-it-to-market-yesterday product development culture puts a lot of pressure on companies to innovate quickly, but creating a safety-first culture can save you from product recalls and failure.
The US Food and Drug Administration (FDA) has issued new guidance that expands the Abbreviated 510(k) Program for medical device development and premarket notification submissions.
Formal and informal reviews may necessitate different things from each of these roles, but we’ve compiled a list of best practices by role to make reviews go quickly and smoothly.
For decades, systems engineers have participated in new product development processes on internal teams, driving complicated projects to market under old rules, methods, and technologies. But today’s highly-competitive markets offer new complexities that no longer work within the old rules of product development.
Jama Connect™ Review Center improves stakeholder alignment, reduces lengthy review cycles, and eases the path to compliance.
Customers leveraging our migration solutions will work with Jama Software consultants to adapt Jama Connect to fit their individual product delivery process, identify and migrate required data, and train teams to quickly achieve sustainable results.
See how medical device development company Össur uses Jama Connect to comply with with international medical device standards like ISO 13485 and ISO 14971.