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91Blog Post

Jama Software Announces Jama Connect™ for Medical Device Development

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Today, Jama Software, introduced Jama Connect for Medical Device Development, a new solution designed to help engineering teams better manage device requirements, risk and design control all on one powerful platform. The newest release makes regulatory submissions and audit preparations a straightforward process, speeding time-to-market deployment with no reduction in quality. Consistent product quality and safety proves to be the top […]

92Blog Post

Expedite Medical Device Launches with Effective Collaboration

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Editor’s Note:  In a time where remote collaboration and distributed teams are quickly becoming the norm rather than the exception, we’re proud to share this post on the value of effective collaboration around medical device design and product development. This article was originally published here on May 5th, 2020 by MedTech Intelligence and written by […]

93Blog Post

TrustRadius Names Jama Connect™ a 2020 Top-Rated Application Lifecycle Management Platform

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  TrustRadius Names Jama Connect™ a 2020 Top-Rated Application Lifecycle Management Platform We are so happy to share that Jama Software has been recognized as a leader among application lifecycle management (ALM) tools for the second year in a row. “We are honored to have received this recognition by TrustRadius. We have the largest team […]

94Blog Post

What Phases are Needed for Developing a Medical Device?

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  What Phases are Needed for Developing a Medical Device? Developing a medical device is an inherently complex process, and one that’s becoming more complicated all the time. In addition to the increasingly stringent regulatory requirements that must be met for FDA approval and/or EU MDR compliance, medical device manufacturers must also navigate ongoing changes […]

95Blog Post

What is Medical Device Risk Management?

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Building and then bringing a medical device to market as quickly as possible—all while preserving acceptable levels of quality and regulatory compliance—requires adept medical device risk management. By minimizing potential risks such as mislabeling and software-related issues, medical device manufacturers make each product safer for the patients who will use them. All of these risks […]

96Blog Post

WEBINAR: TIR45 | An AGILE Approach to Software Regulatory Compliance

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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 […]