- Understand overall EU MDR structure, requirements & key technical terms
- Learn how to correctly classify medical devices including device-drug combinations
- Confidently perform a GSPR applicability analysis
- Learn how to integrate QMS, PMS, Risk Management & Clinical Evaluation
- Identify gaps and priority areas for your regulatory strategy
EnableCE Learn Understanding the EU MDR Training Course
Gain clarity & context on overall EU MDR requirements for your entire regulatory strategy
Course overview
- 17 videos
- Understand overall EU MDR structure, requirements & key technical terms
- Learn how to correctly classify medical devices including device-drug combinations
- Confidently perform a GSPR applicability analysis
- Learn how to integrate QMS, PMS, Risk Management & Clinical Evaluation
- Identify gaps and priority areas for your regulatory strategy
In more detail
Learn how to build a foundation for your entire EU MDR system.
About this course
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We have designed this training course for people who are new to the EU MDR and who want to get started in building a regulatory strategy.
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Instant, on-demand and unlimited access to videos along with updates and additions to the existing training material.
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This course is presented by the CEO of Mantra Systems, Dr Paul Hercock, who has extensive knowledge of the EU MDR. He is an experienced presenter of clinical and technical training.
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You'll take control of your regulatory strategy and manage individual areas of the EU MDR with confidence.
About our courses
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Our training courses are broken up into chapters and short, streamable videos which save your progress automatically. Where relevant, downloadable documents are included to support your learning.
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All our training courses are on-demand and can be completed to your schedule in the comfort of your own workspace. You won't have travel or accommodation costs, or any other expenses usually incurred whilst away from your office.
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You will have unlimited access to your selected training under a Single User Licence. If we update or add anything to the training course material, we will let you know by email. If you require access for multiple team members, please contact us about our Multi User Licences.
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Our EnableCE platform offers training courses and technical document templates that work together to provide a great regulatory support package. Mantra Systems also offers a range of consulting services, MDR resources such as free White Papers, industry focused articles and an EU MDR Compliance Guide.
Start today
You can start your training course immediately after purchase.
Understanding the EU MDR Training Course
- 17 videos
Gain clarity & context on overall EU MDR requirements for your entire regulatory strategy
Single one-off payment £195
Prices shown exclude UK/EU VAT
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For all purchases, you will receive a receipt by email confirming payment.
Templates & tools:
You will receive an email containing a link to download your files.Training courses:
You will go through the account set up process to access the training course platform.Training course + template package:
You will go through the account set up process to access the training course platform. Within one working day you will receive an email to download your template(s).
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Learn CER Writing Training Course
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Medical Device Regulation Resources
Our Medical Device Regulation Resources contain information and guidance on a wide range of aspects across the regulatory landscape.
For further guidance or any specific enquiries, please contact our specialist consultants.