Choose another country to see content specific to your location

//Select Country

Risk assessment and management in Additive Manufacturing

Get approval for Am products

PAID LIVE VIRTUAL TRAINING SCHEDULE

  • 13th to 14th October 2020: Risk assessment and management in Additive Manufacturing (AM) training
    2 pm to 6 pm SGT | 8 am to 12 pm CEST | 2 Days
  • 26th to 27th January 2021: Risk assessment and management in Additive Manufacturing (AM) training
    2:30 pm to 6:30 pm SGT | 8:30 am to 12:30 pm CEST | 2 Days

This module is part of a bundled training course, the iAM Quality Manager certificate line.

ABOUT THE COURSE

This paid course focuses on how to properly conduct an AM-specific Risk assessment and management.
 
The training is intended to provide a holistic overview of risk assessment and management for AM products,the required know-how and input how to conduct the risk assessment with examples from the medical sector but the topics discussed are applicable for all. Risk management will cover the systematic management of the analysis, evaluation and control of risks. The second part of the training will be a workshop to discuss specific situations in conjunction with the new input, so that you will have first results and ideas that will be useful for your specific situation and can continue working on them in your company in an effective manner.

Using the medical industry as an example, the quality management standard ISO 13485 explicitly requires risk management and all associated documentation for the entire product realization process. The requirements in ISO 14971 for this purpose must in turn be transferred to additive manufacturing technology. 

Duration: 2 Virtual Sessions (4hr each)

WHAT WILL YOU LEARN FROM THE COURSE?

At the end of the course, participants will be able to:
This training enables you to implement an AM-specific Risk assessment and management approach in you company. You will be able to realise and optimise parts, processes and process chains and handle their risks – especially required in regulated industries like medical or aerospace. 

Topics to be covered in this course include:

  • Risk assessment for AM-Products

  • Risk assessment for AM-Process-Chains

  • AM-specific risk management

  • Focus on medical sector

  • Workshop (discuss specific situations and cases, possible solutions to you company to proceed in an effective manner and deepen the new gained knowledge)

  • Summary and outlook

WHAT IS THE COURSE METHODOLOGY?

Participants will learn through lectures, case studies, group exercises, discussions and workshop elements.

WHO SHOULD TAKE THE COURSE?

This course is specially designed for quality and production managers as well as risk and product managers who are or who want to become active in AM serial production.


Prerequisite: Basic understanding of AM. It is recommended to attend the Quality and Production Management for AM training in conjunction with this training. 

 

WHO IS THE COURSE ADVISOR?

The course content and structure are designed by the domain experts from TÜV SÜD.

With immense experience and knowledge in the relevant standards, our team of product specialists and technical experts at TÜV SÜD, developed the course content based on current business landscape and market requirements.

 

What are the benefits of enrolling in this course?

  • Comprehensive, product-specific compact knowledge about risk assessment using Additive Manufacturing
  • Learn how to manage AM specific risks
  • Get an overview of the risk management criteria, e.g. mentioned in ISO 14971 (for medical)

Next Steps

Select Your Location

Global

Americas

Asia

Europe

Middle East and Africa