Medical Devices 2011 - Don't RISK to ignore RISKS. Understanding ISO 14971

Why Should You Attend:
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.