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EU MDR Training Courses on the European Medical Device Regulation (2017/745)
EU MDR Training Courses on the European Medical Device Regulation (2017/745)
Comply Guru offer EU MDR Training that is available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization learn about the European Medical Device Regulation (2017/745). We were the first training provider to offer IRCA Certified EU MDR Training in the world...
EU MDR Training Types
The European Medical Device Regulation (2017/745) has replaced the Medical Devices Directive (93/42/EEC) as the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.
Comply Guru offer the following types of EU MDR training courses depending on the target audience and/or learning objectives, including:
Essentials Training is for non-QARA personnel who need a short, general overview of the EU MDR (2017/745) for awareness purposes.
Practitioner Training is for those who are new to the Regulation but working in Quality or Regulatory Affairs and need a broad understanding of the EU MDR (2017/745).
Auditor Training is for those who are familiar with the regulation, and already trained as ISO 13485 Lead Auditors, and now need formal training on how to audit under the EU MDR (2017/745).
This course will provide learners with the knowledge and skills required to perform audits of medical device quality management systems (MD-QMS) against the European Union’s Medical Device Regulation (EU 2017/745) in accordance with ISO 19011 and ISO 17021 as applicable.
This online course takes you through the new European Medical Device Regulation (2017/745), not just from an industry perspective, but also from a Notified Body perspective. It has been specifically designed for Quality & Regulatory Professionals who are new to the Regulation.
This course provides clarity on the role and responsibilities of the Person Responsible for Regulatory Compliance (PRRC) introduced under Article 15 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).
Comply Guru offer a European Medical Device Regulation (EU MDR 2017/745) Essentials Course for organizations looking for a concise, high-level introduction for their staff.
2 hours Comply Guru
$ 395.00
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