Examples of Failure Mode and Effects Analysis in a sentence
A Failure Mode and Effects Analysis (FMEA) shall be conducted to investigate possible risks and evaluate them in terms of importance, probability of occurrence and likelihood of detection.
During "Prototype" and "Pre-Production" Program Management Phases, prior to serial production shipments, APQP documents like, for e.g., Process Flow Diagram, Design and/or Process Failure Mode and Effects Analysis (D/PFMEA), Controls Plans, Measurement System Analysis (MSA), Inspection Reports, and Capability Studies, Feasibility Analysis, etc.
Many aids are available, including experience, engineering codes, checklists, detailed process knowledge, equipment failure experience, hazard index techniques, What-if Analysis, Hazard and Operability (HAZOP) Studies, Failure Mode and Effects Analysis (FMEA), and Preliminary Hazard Analysis (PHA).
As detailed in paragraph 5.2.2 below, standard techniques such as Hazard and Operability (HazOp) study and Failure Mode and Effects Analysis (FMEA) can be, and are, used for this purpose.
Including but not limited to:• Develop and review Process Failure Mode and Effects Analysis (PFMEA) when required by HAU.• Develop a Process Control Plan.Detailed PFMEA and control plan training materials and forms may be requested from HAU through the responsible buyer or SQE.
The latest edition of the following AIAG reference manuals are used to develop this Supplier Quality Manual: Advanced Product Quality Planning and Control Plan (APQP) Materials Management Operations Guideline (MMOG) Measurement Systems Analysis (MSA)Potential Failure Mode and Effects Analysis (FMEA) Production Part Approval Process (PPAP) Statistical Process Control (SPC) Additionally, ISO 9001:2015 and IATF 16949:2016 are used in the development of this Supplier Quality Manual.
The com- munication layer is characterized by the undirected edge set EW and a weighted adjacency matrix W∈ Rn×n, with entrieswi j = 0 ⇐⇒ (i, j) ∈EW .
The primary Safety Evaluator applies his/her individual expertise gained from evaluating medication errors reported to FDA, considers all aspects of the name that may be misleading or confusing, conducts a Failure Mode and Effects Analysis, and provides an overall decision on acceptability dependent on their risk assessment of name confusion.
Requirements include: Production Part Approval Process (PPAP), Advanced Product Quality Planning (APQP), Potential Failure Mode and Effects Analysis (FMEA), Measurement Systems Analysis (MSA) and Statistical Process Control (SPC).
In this case, the analysis of the safety data integrity requirement and the security data requirement result in a single solution that satisfies both requirements (MAC).Security can hardly be measured and modelled statistically, which prevents safety methods being adopted as they are into the security domain, i.e. FTA or Failure Mode and Effects Analysis (FMEA) have to be refined and extended for security analysis (FMVEA).