Tag: DOORS Next Generation

Looking for help to get started with IBM DOORS NG?

Post author By Imran Hashmi
Post date December 17, 2020

Looking for help to get started with IBM DOORS NG?

IBM Rational DOORS Next Generation is a web-based requirements management solution for complex software and systems engineering environments. This playlist is for anyone who wants to learn about IBM Rational Doors Next Generation. The topics are at a high level, providing an overview of key use cases and product features.

More information: http://goo.gl/eZ0cI Using DOORS NG with OSLC: https://jazz.net/library/article/1197 Latest DOORS NG information: https://jazz.net/products/rational-do… Intermediate list of RDNG videos: https://www.youtube.com/playlist?list… Advanced/Administration list of videos: https://www.youtube.com/playlist?list… Configuration management videos: https://www.youtube.com/playlist?list…

Requirements Design Testing Workflow

Demo: ALM for Medical Devices IEC 62304 ISO 13485 ISO 14971

Post author By Imran Hashmi
Post date December 4, 2020

IBM ApplicationLifecycle Management or ELM Engineering Lifecycle Management for Medical Devices IEC 62304 ISO 13485 ISO 14971

Tags: ALM, Compliance, DOORS Next Generation, FDA Compliance, IBM ELM, IBM Engineering Lifecycle Management, IEC-62304, ISO-13485, ISO-14971, Medical Devices

Tags ALM, Compliance, DOORS Next Generation, FDA Compliance, IBM ELM, IBM Engineering Lifecycle Management, IEC-62304, ISO-13485, ISO-14971, Medical Devices

Design Requirements Testing Workflow

Streamlining medical device design for US FDA Compliance

Post author By Imran Hashmi
Post date December 1, 2020

Three key themes to set up your Medical Device Design engineering for success

IBM Engineering Medical device manufacturers must innovate to succeed. To grow, manufacturers must deliver innovative, safe, and fully compliant Medical Devices. This means adhering to increasingly rigorous regulatory standards like ISO 13485, IEC 82304-1, ISO 14971, IEC 60812, IEC 62304, ISO 60601, IEC 61508, 21 CFR 820.30, and 21 CFR 11 driven by both EU's MDR and the US FDA regulations. IBM helps to:

Reduce time to innovation

−Adopt agility at scale that meets the needs of each part of your development team such as SAFe®

−Reduce time to market with strategic reuse by creating and managing product variants across multiple product lines Improve quality−Achieve transparency and traceability for design control as a by-product by creating work products in a controlled environment

−Use AI to validate quality of requirements reduce cost of Compliance−Understand status, responsibilities, audit trial and history for design control work products at every stage of the development−Automatically generate high-quality documents from multiple sources to support compliance and audit requirements

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Tags: ALM, Compliance, Design, DOORS Next Generation, FDA Compliance, IBM, IBM Doors NG, Medical Device, requirements-management, SDLC, US FDA

Tags ALM, Compliance, Design, DOORS Next Generation, FDA Compliance, IBM, IBM Doors NG, Medical Device, requirements-management, SDLC, US FDA

Requirements Design Testing Workflow

Introduction to IBM Rational DOORS Next Generation

Post author By Imran Hashmi
Post date November 30, 2020

Check out the DOORS Next Generation free trial today and see how it has requirements management redefined: http://ibm.co/DNGTrial. In this video Ian Zimmerman from IBM teaks you through why you should use a requirements management tool, current DOORS vs. DOORS NG, key features of DOORS NG, and then a demonstration of DOORS Next Generation….