EU MDR 2017/745 Training Course
Gain confidence in implementing the EU MDR!
The EU MDR has certainly caused significant impact to the medical device industry. We are still learning some of the nuances, and with the extended time frame for compliance, some companies are still navigating their way through the requirements.
If you are unsure of what is required, then join us as we explore the regulation and make sense of what you need to do in a practical way, with easy to understand examples.
Receive useful advice on updating your quality system, overseeing economic operators, addressing labeling and handling technical documentation.
Date: 17 - 20 February, 2025 (4 half days)
The EU MDR has certainly caused significant impact to the medical device industry. We are still learning some of the nuances, and with the extended time frame for compliance, some companies are still navigating their way through the requirements.
If you are unsure of what is required, then join us as we explore the regulation and make sense of what you need to do in a practical way, with easy to understand examples.
Receive useful advice on updating your quality system, overseeing economic operators, addressing labeling and handling technical documentation.
Date: 17 - 20 February, 2025 (4 half days)
Time: 13:00 - 17:00 GMT | 8:00 - 12:00 EST
RAC Credits: 12
SOLD OUT !
RAC Credits: 12
SOLD OUT !
What's included?
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Your own learning portal
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Course recordings
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Free 1-2-1 with the trainer
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Live sessions
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PDF materials
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Self paced modules
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Certificate of completion
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Access to a community
Learn with a community
Social learning is a powerful tool that enables individuals to learn from each other through observation, communication, and collaboration.
Using our community, people can more efficiently acquire new knowledge, skills, and behaviors.
Using our community, people can more efficiently acquire new knowledge, skills, and behaviors.
Assessments & Feedback
Assessments and feedback are essential components of the learning process, offering valuable insights into progress.
All of our courses use knowledge checks and practical peer learning throughout to reinforce understanding.
All of our courses use knowledge checks and practical peer learning throughout to reinforce understanding.
- Meet the trainer
Rod Beuzeval
Rod’s experience has involved providing regulatory strategy from product development to worldwide market registration, creation of technical documentation, implementation of full 13485 compliant QMS systems, standards compliance, clinical evaluations, risk management files, project management and remediation activities. Rod has also spent time working for a notified body, conducting audits against ISO 9001, ISO 13485, 21CFR820, MDSAP, cGMP and GDP.
Let's discuss your
training needs.
Thank you!
Frequently asked questions (FAQs)
Who should attend this course?
This course is ideal for medical device professionals, including regulatory affairs specialists, quality assurance managers, and anyone involved in compliance. It's suitable for both those new to the field and experienced professionals looking to deepen their understanding of the EU MDR requirements.
How will this course help with updating our quality system to comply with the EU MDR?
This course will guide you through key areas related to EU MDR compliance:
Such as Understanding what your QMS must include, ensuring your PMS systems align with the MDR, the impact of MDR on supplier controls and the discovery of necessary technical documentation.
Will I receive a certificate after the course?
Upon successfully completing this training, you will receive a digital certificate. This certificate can be used to showcase your clinical knowledge to employers and Notified Bodies.
