Library
Medical Device Reliability Program
The FDA has their Design Controls in the Code of Federal Regulations Title 21 Part 820.30, then for outside the US, we have ISO 13485:2003 Medical devices – Quality management systems..
- Filetype: pdf
- Publish date: 2011-05
- Keywords:Product Development Planning
Risk Assessment Using Design Review Based On Failure Mode
Sustainability requires better reliability possibly improved by risk assessment during product development. Besides FMEA Design Review Based on Failure Mode is a structured method to perform risk assessment. Experience and best practice of this method.....
- Filetype: pdf
- Publish date: 2011-01
- Keywords:RAMS 2011 Proceedings, Product Reliability, Design Review, Product Development Planning
Model-driven Automated Software FMEA
This paper will describe how software FMEA can be automated both for low-level languages intended for safety critical embedded systems, and also for model-driven software developments...
- Filetype: pdf
- Publish date: 2011-01
- Keywords:RAMS 2011 Proceedings, Product Reliability, Design Review, Product Development Planning, Software Reliability
Using FMECA to Design Sustainable Products
For many years now Failure Mode, Effects and Criticality Analysis (FMECA) has been a very effective technique used for identifying possible failures and mitigating their effect. Although mainly used to identify failures as.....
- Filetype: pdf
- Publish date: 2011-01
- Keywords:RAMS 2011 Proceedings, Product Reliability, Design Review, Product Development Planning
Effective Oversight
The reliability group of a large defense contractor must report to management their progress in meeting Design for Reliability (DFR) objectives. Management is requesting metrics that they can use to track DFR milestones at each milestone in the phase.....
- Filetype: pdf
- Publish date: 2011-01
- Keywords:RAMS 2011 Proceedings, Product Reliability, Design Review, Product Development Planning
Proactive Risk Management
How to Conduct the Failure Investigation before the Event
Here is a simple strategy for proactive risk management that can allow any cross functional team to evaluate products and process for the "hidden monsters" that can do so much damage...
- Filetype: pdf
- Publish date: 2011-01
- Keywords:Product Development Planning
Transcending Performability for System Attributes’ Consistency
For complex systems where different perspectives need to be addressed, maintaining consistency among various system analyses is a challenge. A framework that supports a global view to govern various analyses is critical for integrity of system analyses...
- Filetype: pdf
- Publish date: 2010-01
- Keywords:RAMS 2010 Proceedings, Reliability Model, Requirements Flow Down, Product Development Planning
Using Risk Assessment to Mitigate New Business Demands
Global market requires compliance with legal and regu..
- Filetype: pdf
- Publish date: 2010-01
- Keywords:RAMS 2010 Proceedings, Life Cycle Cost, Product Development Planning, Fault Tree Analysis
Using Electronic Design Automation Throughout The Product Life Cycle
Several classes of ongoing analysis challenges regularly arise during production maturation of programs in military,aerospace, telecommunication, and medical areas...
- Filetype: pdf
- Publish date: 2010-01
- Keywords:RAMS 2010 Proceedings, Conceptual Design, Product Reliability, Product Development Planning, Software Reliability
Reliability Engineering As a Practical Application to Improving System Performance – From Concept to System Retirement
Reliability, availability, and maintainability (RAM) are three very important and necessary disciplines that must be applied within the system engineering process to ensure program success...
- Filetype: pdf
- Copyright: 2011
- Keywords:Design Reliability, Maintainability, Product Development Planning, Product Reliability, RAMS 2011 Proceedings, Reliability
