May 2 @ 8:00 am - May 3 @ 5:00 pm€699
Introduction to our two day Risk Management Training
The requirements for Product Risk Management as it pertains to all stages of a Medical Device Lifecycle is outlined in ISO 14971. The emphasis on the Risk Management process extends from Conformity and Compliance Assessments to assurances that Outsourced Processes, including Suppliers are thoroughly, adequately and appropriately audited with a Risk-based approach.
Who should Attend:
All personnel involved in areas relating to Quality, Production, Engineering, Supplier and Outsourced Process Management should be conversant with these requirements to provide assurance of Competency in Medical Device Product Risk Management.
This intensive course will focus on the requirements of the ISO 14971 and will demonstrate Risk Management practices that reflect best in class practices.