This Buyer’s Guide incorporates insights from Jama Software’s more than ten years of experience partnering with forward-thinking product development teams. We’ve designed a platform to help automotive development teams reduce barriers to compliance for their automotive manufacturing process.
This allows automotive developers to:
Align to industry regulations quickly
Simplify functional safety compliance process
Accelerate time to market
Changing market dynamics requires a modern and collaborative approach to requirements management. See why customers on G2® prefer Jama Connect over IBM® DOORS® Next and what migration looks like.
Download this whitepaper to learn more about top automotive industry challenges and how to solve them, and the evolution of functional safety in modern automotive development.
What is ASPICE? Download our Automotive SPICE guide for a comprehensive look at ASPICE goals, requirements, and achieving compliance in automotive development.
Download this eBook to see how software teams are using Jama Connect’s single requirements platform to accelerate time to market.
Download this eBook to see how software teams in financial services and insurance industries are using Jama Connect’s single requirements platform to accelerate time to market.
Download this eBook to learn how medical device developers can prepare and implement the necessary changes to achieve compliance with the new EU MDR regulations.
In this eBook, learn to reduce project risk in the development process by implementing Living Requirements™ management forming a digital thread through siloed development, test, and risk activities.
This guide shows you how effective requirements writing and requirements management helps improve project outcomes and reduce late-stage rework and budget overruns.
In this eBook, our experts explain how to write clear, concise requirements that drive greater transparency, less rework, and accelerated product development.
Learn what to look for in a medical device development platform to help accelerate the development of safe, high-quality devices while managing ever-shifting complexities and regulations.
Learn how optimizing your engineering team’s collaboration can streamline the product development process, add business value, and provide a competitive edge.
For this information-packed eBook, Jama Software teamed up with Beanstock Ventures to weigh in on trends and predictions for medical device development in the new year and beyond.
Read this guide to learn the purpose of ISO 13485 and requirements for adherence, the difference between ISO 13485 and other medical device standards, and get key steps to adoption and certification.
Medical device companies must evaluate how their development process stands up to the challenge of increasingly connected technologies and strict regulation.
Get a brief overview of four Jama Software customer stories. Rimac car manufacturer, Jones Lang LaSalle Incorporated (JLL), Deloitte, and RBC Medical Innovations each faced unique challenges.
Creating a centralized place to manage reviews eliminates the need for lengthy meetings or back and forth emailing, making reviews more efficient and scalable.
This eBook covers the importance of tracing requirements without the headaches and risks of a traceability matrix in Excel.
Jama Connect can address the particular priorities and concerns of each team across your organization. Learn what each team cares about most, what sets Jama Software apart, and how to demonstrate ROI.
Jama Connect is the leading solution for requirements, risk and test management
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