Risk Management Activities during Design Input

Learn how to use tools such as Preliminary Hazard Analysis to eliminate expensive design changes that occur when problems are discovered during Design Verification and Design Validation. Risk Management Activities can lead to reduced cost and reduced time to market when conducted during the Design Input phase of product development. Learn how to use tools such as Preliminary Hazard Analysis to eliminate expensive design changes that occur when problems are discovered during Design Verification and Design Validation.

Find out about data sources that can be mined to reduce risks early in the design process thus giving developers more information to aid in product design.

Areas Covered in the seminar:

• Preliminary Hazard Analysis a tool for improved product design.

Who Will Benefit:

This webinar will update personnel at medical device companies on the new standard and point them to the additional information available in the newly revised document. The information will assist in meeting various national and global regulatory requirements for medical devices.

Design personnel using risk management during development of new medical devices.

Quality managers responsible for integrating risk management into quality systems.

Regulatory and compliance personnel who develop premarket filings and technical files for medical devices.

Personnel responsible for verification and validation activities.

Quality system auditors.