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What is FMEA (Failure Mode and Effects Analysis)? Failure Mode and Effects Analysis (FMEA) is a structured process for determining potential risks and failures of a product or process during the development phase. FMEA teams examine failure modes—those potential points of failure in a product or process — and what the failure effects (risks, harm, […]
Toys to Tools – Keeping Pace with eVTOL Certification Standards Today’s market for electric vertical takeoff and landing (eVTOL) is one of the most innovative and fast-moving in the aerospace industry, so keeping pace with ever-changing eVTOL certification standards is no easy endeavor. eVTOL Applications The military led the way in eVTOL by transforming drones […]
Editor’s Note: This posts on autonomous vehicle development was originally published here by EE Times and written by Junko Yoshida. While this post was published in 2020, the content is still relevant to AV development in 2021. How many safety standards does it take to screw in the lightbulb in a highly automated vehicle? A few years ago, […]
Ensuring Aerospace Compliance to Regulatory Requirements We are in a time of unyielding technological development. It is not unlike the “giant leaps” made by the US Space program in the 1960s. The technology available to us in our everyday lives and certainly in the Aerospace and Defense industry is staggering. Think about when you got your first cell phone. Remember […]
In this post, we review the details of the latest product roadmap enhancements related to baselines and how these changes benefit our customers.
In this post, experts from LHP Engineering Solutions examine the difference between being ISO 26262 compliant and being ISO 26262 certified.
In this post, experts examine how functional safety requirements fit into the larger view of organizational QMS aligned with IATF 16949.
In Part I of our six-part automotive series, our experts discuss how to accelerate automotive SPICE (ASPICE) capability with Jama Connect for Automotive.
Based on our work with hundreds of medical device developers, we’ve compiled this guide to navigating the complexity of medical device compliance.
Medical device manufacturers have a lot to keep track of these days. Between ongoing device development and preparing for the impending EU MDR, it’s more important than ever to maximize every partnership.