THIS WEBINAR ON FAILURE MODE AND EFFECTS ANALYSIS 2015 - Failure Mode and Effects Analysis- FMEA for Medical Devices

Website http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500997?expDate=Sep10_2015_Medical | Edit Freely

Category Failure Mode and Effects Analysis, FMEA for Medical Devices, FMEA for Design Improvement, FMEA for Design Control, Medical Device risk analysis and risk mitigation, Safe Medical Devices Act, Section 820.30, Medical Device GMP

Deadline: September 09, 2015 | Date: September 10, 2015

Venue/Country: online Webinar, U.S.A

Updated: 2015-09-01 18:31:48 (GMT+9)

Call For Papers - CFP

Instructor: Dev Raheja

Product ID: 500997

Description

In this webinar "Failure Mode and Effects Analysis for Design Excellence in Medical Devices," attendees will learn how to design medical devices that enhance reliability, safety, durability and serviceability. They will also gain a thorough understanding of both the Design FMEA, and the Process FMEA.

Areas Covered

The wrong practices in FMEA

FMEA procedure-the right way

Using FMEA to improve the design specifications

New paradigms for design improvement

Using FMEA for verifying design outputs

Using FMEA for design inputs

Avoiding wrong practices FMEA practices for efficient results

Identifying critical design features

Using best strategies to mitigate risks

FMEA for Planning Design Validation

FMEA to avoid manufacturing defects

Why Should you Attend

This webinar will detail how you can design medical devices that enhance reliability, durability, safety, and serviceability. The course will cover both the Design FMEA, and the Process FMEA. Risk analysis is now required by law (GMP). Identification of device design problems prior to distribution eliminates costs associated with warranties, product recalls, and product validation.

FMEA (Failure Modes and Effects Analysis) can reveal missing requirements, vague requirements, missing functions, and point out component and manufacturing problems well before process validation. These in turn reduce life cycle costs and reduce the time to market. Design FMEA serves as a central document in the design control process. Similarly the Process FMEA serves as the central document in the process validation qualification.

Objectives of the Presentation

Learn to avoid warranty costs

Understand how to use FMEA correctly

Avoid classic mistakes that waste time and produce ineffective results

Capture new risks

Learn the art of elegant problem solving

Learn to minimize inspection and testing

Help management in risk evaluation and decisions on marketing the product

Who can Benefit

This course is designed for all technical employees. This is particularly important for all managers because 85% device defects are said to be the result of poor management practices. The following personnel will benefit from the course:

Quality assurance supervisors

Senior Managers

Design Engineers

Production Supervisors

R&D Engineers

Quality Professionals

Compliance Professionals

Regulatory Professionals

Manufacturing Engineers

Quality Auditors

Production Engineers

Document Control Specialists

For Registration -

http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500997?expDate=Sep10_2015_MedicalDevices=Channnel=ourglocal

Note : Use coupon code 1371 and get 10% off on Registration