Failure Mode and Effect Analysis (FMEA) – Risk Analysis and Management

Thursday, Apr 27, 2017 at 10:00AM - 1:00PM

Event Details

Failure Mode and Effects Analysis (FMEA) is a systematic method for preventing failure through the discovery and mitigation of potential failure modes and their cause mechanisms. Actions are developed in a team environment and address each high: severity, occurrence or detection ranking indicated by the analysis. Completed FMEA actions result in improved product performance, reduced warranty and increased product quality.

Failure Mode and Effect Analysis (FMEA) is a powerful risk assessment technique that today has broad applicability to many industries including manufacturing, healthcare, medical device, food and drug, software, and services. Risk analysis and management are both requirements in many quality, safety and environmental standards such as ISO 9001, 14001, 18001, AS9100, and TS16949. FMEA can help an organization comply with those requirements.

Objectives of the Presentation
  • Explain how FMEA's fit within a Risk Management System
  • Create an FMEA to include Risk Identification, Risk Analysis, Risk Estimation and Risk Control
  • Identify potential failures and their effects
  • Prioritize failure modes
  • Create action plans to eliminate or control risks
Why Should you Attend
Using a systematic approach initially popularized in military circles, FMEA is a risk analysis and management tool by which we examine potential product and process failures and, in turn, determine the need for and way to address means to prevent or lessen the impact of those potential failures.

Our FMEA webinar will ensure that the use of the FMEA tool will build a culture that emphasizes prevention of issues/problems before they occur. The FMEA tool helps to spot risks early on in the development of processes and can be used throughout the risk management process to identify, analyze, evaluate and reassess risk. This information can also be used to document risks and suggest performance and process improvements.

Areas Covered
  • Define types of FMEA's
  • The important benefits of FMEA
  • Be familiar with components of FMEA
  • Understanding process requirements
  • Explanation of the principles of Risk Analysis
  • FMEA's at the design stage
  • FMEA's of processes
  • Identification of the causes and effects of failure
  • How to Manage designated personnel with the skills to conduct and complete an FMEA of products or processes
  • How to select cross-functional teams
  • Case studies of typical situations and applications
Who will Benefit
  • Design Managers
  • Design Engineers
  • Manufacturing Personnel
  • Process Managers
  • Process Engineers
  • Quality Assurance Personnel
  • Reliability Research Personnel
  • Development Department
  • Safety Engineering Personnel & Product, process, design, and R&D engineers and scientists.

For Registration


Note: Use Promo code DE5YU and get 10% off on registration (Valid till APRIL 30th 2017)

Organization Details

Online Compliance Panel (OCP) creates and delivers comprehensive industry relevant training sessions. These sessions are simple, interactive and cost effective. We are a predominantly web based information exchange forum. Live interactions on compliance training make the process holistic and effective. OCP largely emphasizes in offering regulatory compliance training to compliance professionals on varied topics. These primarily include risk management, quality management, corporate compliance and other regulatory compliances. Some of our primary areas of focus include advancement and updates in regulatory compliance, best practices and market trends.

We strive to incorporate high standards in developing a culture facilitating exchange of ideas resulting in functional excellence. OCP believes in nurturing ideas and thought processes through innovative e-learning methodologies. Our products and services are designed to offer customized solutions to industry and market. We bridge the gap between experience and knowledge thus delivering original and creative content.

Our objectives of employing interactive mediums ensure effective communication and mutual exchange of ideas. OCP closely follows best practices and regulatory trends in the global compliance scenario. We also observe and communicate trends witnessed in FDA, ISO regulations, process and design validation. All updates and additions to important laws can be accessed by our customers in real time.

Our mission is to empower compliance professionals through effective online training sessions. Our world class training methodologies stem from comprehensive understanding of client requirements. The content conforming to FDA and ISO standards is developed by well qualified and experienced industry leaders. Our offerings will exceed expectations and add value to your investment.

The content in various categories such as medical devices, pharmaceuticals and biotechnology will raise the bar in terms of quality already on offer .We hope to contribute to the creation of responsible organizations creating benchmarks in quality, integrity and transparency.

Online Event
38780 Tyson Lane, Apt 210
Fremont 94536

Starts April 27, 2017 at 10:00AM - 1:00PM

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Contact Information

Organization: Online Compliance Panel LLC

Event Contact: OCP Panel

Phone: 15108575896