Risk Management Techniques for Medical Devices 2018

Topics

• Integrating the new standard with ISO 13485 as part of your overall QMS
• Overview of the ISO14971 standard as it applies to medical device companies
• Stages of Risk Management as well as Tools and Techniques
• Conducting a review of the intended use of your device
• Judging the probability that harm may occur from those hazards
• Identifying hazards in your product or production process, and estimating their severity
• How to control those risks and monitor the effectiveness of the controls put in place

Who should Attend

• Manufacturing Engineer
• Design Engineer
• R&D Personnel
• Quality Engineer
• Quality Managers
• R&D Project Managers