Risk Management for Medical Devices 2016 is a webinar that covers topics such as:
- 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
- Modifying your design and development process to incorporate ISO14971
- Conducting a review of the intended use of your device
- Identifying hazards in your product or production process, and estimating their severity
- Stages of Risk Management as well as Tools and Techniques
- How to control those risks and monitor the effectiveness of the controls put in place
- Judging the probability that harm may occur from those hazards
Risk Management for Medical Devices 2016 is intended for attendees from:
- Technicians involved in new product development and manufacturing of medical devices
- Engineers
- Auditors
- Quality Managers
- Personnel involved in failure investigations and CAPA
- Regulatory Affairs personnel
- Design Engineers
- Validation professionals
- Project Managers involved in design and development
