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The ISO standard of 14971:2019 has been published a few months ago. What impact do the new revisions of the standards ISO 14971:2019 and ISO/TR 24971:2020 have on risk management? How does the standard relate to MDR? If you look at the details of the standard, there are numerous details and possibilities to improve important contents in risk management sustainably. In the E-Learning you will get to know the innovation of ISO 14971:2019 as well as an overview of ISO/TR 24971:2020. You will understand how to implement the changes of the new ISO 14971:2019 in your company. The connections between MDR and risk management will be explained to you. At the end of the E-learning you can test your knowledge in a short knowledge test.
Duration of the training: 60 minutes
Learning mode: Self-Paced
Upon successful completion of this E-learning module, you will have a clear understanding of the following:
The cumulative duration of the programme is 60 min., after which you will be required to pass a quiz to receive your internationally recognised e-certificate with a unique ID.
This course is specially designed for:
This course is specially designed for Product and process developers, medical device manufacturers and their suppliers, employees in quality management and regulatory affairs, QM representatives, safety representatives for medical devices, as well as consultants and service providers.
Designing the content course and structure are domain experts from TÜV SÜD’s Digital Academy Approval Board.
Based in various locations worldwide, these are specialised trainers who have been working with top-notch employers and industry associations to achieve business excellence with asset management system implementations.