ISO: 14971 Risk Management – One day Course - Virtual Classroom 

Sept 2 2021 

€699  Price includes training, all training materials, certification and refreshments during the training where applicable.  Need a quote for In-house Training email us today info@iqc.ie  Introduction  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.  This intensive course will evaluate and focus on the requirements of the ISO 14971 in detail and will demonstrate Risk Management practices that reflect best in class practices. During the 2 days participants will acquire knowledge and skills to implement an effective Risk Management system in conformance to ISO 14971. Risk Management, like any other system, evolves over time within a company as knowledge grows and frequent reviews are conducted. Hence, the best place to practice and extend your experience is in reviewing one’s current system, conduct a gap analysis and determine if current established requirements are sufficient to meet applicable regulatory requirements.  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.  Cancellations Places cancelled within 10 working days of commencement must be paid in full. Substitutions may be made at any time at no additional charge.