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

Nov 26 and 27 2020 

€549  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. 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. 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. 
 
During the 2 days participants will acquire knowledge and skills to implement an effective Risk Management system in conformance to ISO 14971. Risk Management, similar to 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. 
 
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. 
 
Need a quote for in-house training email info@iqc.ie or phone +353 (0) 1-204 0646 
 
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. 
Course Objectives 
Describe the Purpose of a Risk Management system and explain the Risk Management Process elements. 
Explain the purpose, content and interrelationship of ISO 14971, ISO 13485, 21CFR820, MDSAP and EU MDR. 
Interpret requirements of ISO 14971. 
Define risk management. 
Describe most frequently used risk assessment tool. 
Define basic risk management terms. 
Identify risk management responsibilities. 
Describe the benefits of risk management. 
 
Day 1 
Standards - Overall intent of ISO 14971 in relation to ISO 13485, 21CFR820 and MDSAP; 
Understanding of Risk Based Approach V Risk Management; 
Risk Management Overview; 
Risk Management Definitions; 
Team Exercises. 
Risk Management Process Elements:  Planning; 
Analyzing;  Evaluating; 
Assessing;  Controlling; 
Monitoring;  Reporting; 
Post Market Surveillance;  Management Responsibility; 
Risk Management Lifecycle; 
Overview of Frequently Used Risk Management Tools; 
 
• Application of RM to all aspects of Quality, Production and associated activities. 
 
Day 2 
• Risk Management - Recap Day 1; 
• Differentiating between Intended Use and Indications for Use; 
• Case study exercises on applying ISO 14971; 
• Risk Management Tools and sample Exercises; 
• How to identify and document Harms, Hazards and Hazardous situations; 
• Top Level - How to document Risk Management Plan; 
• Top Level - How to conduct a Hazard Analysis; 
• Top Level - How to cascade harms in a Fault Tree Analysis; 
• Top Level - How to perform a PFMEA (Product/Process); 
• Top Level - How to document Risk Management Report; 
• Course Evaluation; 
 
Delivered by Pharma/Biopharma Experts 
 
 
 
Risk Management ISO 14971| Virtual Classroom 26 & 27 Nov 2020
€699.00
The requirements for Product Risk Management as it pertains to all stages of a Medical Device Lifecycle is outlined in ISO 14971.
 
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