MEDICAL DEVICES 2011 - Don't RISK to ignore RISKS. Understanding ISO 14971

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Category Medical Devices,conference,event,Webinar

Deadline: March 31, 2011 | Date: March 31, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2011-02-02 18:05:00 (GMT+9)

Call For Papers - CFP

Medical Device Companies are using different tools to identify and manage the risks but sometimes companies lack the over all process to connect the dots. This gap has resulted in several field failures and significant recalls of the products due to inappropriate prioritization of risks involved. ISO 14971 provides a comprehensive model to not only identify the risk, but also to prioritize and mitigate the risks to as low as reasonably possible. The scope includes the entire product realization process including the afterlife disposal of the devices.

This 3.5 hr webinar will discuss the key elements of the risk management process, FDA recognized risk management model and how to connect different activities to better understand the product and process risk and risk mitigation.

Learning Objectives:

FDA recognized Risk Management Model

Detect risks early in the Design & Development phase

Improve product performance by mitigating risks

Helps differentiate your product from the competition

Helps the team and management talk the same language

Effective way to prioritize the risks

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.