Online EU MDR 2017 745 Training on the European Medical Device Regulation

Comply Guru are the first in the world to offer Multi-Accredited Online European Medical Device Regulation (MDR 2017/745) Training in the United States with the Chartered Quality Institute (CQI), International Registrar of Certificated Auditors (IRCA) and the Regulatory Affairs Professionals Society (RAPS) offering credentials for the Medical Device Industry that are globally recognized.

The European Medical Device Regulation (MDR 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 different types of EU MDR training courses depending on the target audience and training needs. We can also tailor training to meet your company’s specific needs or requirements. Our courses are available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization master the European Medical Device Regulation (MDR 2017/745).

CQI-IRCA Certified Course Exemplar Global Certified Course RAPS Certified Course
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EU MDR Requirements Training for Practitioners working with the European Medical Device Regulation (2017/745)
4.6 ★★★★★ 386 Reviews
EU MDR Medical Devices

EU MDR Requirements Training

24hrs
CQI-IRCA Certified Course RAPS Certified Course
Price: $1195.00

EU MDR Requirements Training for Practitioners 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 and regulatory Professionals who are new to the Regulation.

EU MDR Lead Auditor Training for the European Medical Device Regulation (2017/745)
4.9 ★★★★★ 21 Reviews
ISO 19011 ISO 17021 EU MDR Medical Devices

EU MDR Lead Auditor Training

24hrs
CQI-IRCA Certified Course
Price: $1995.00

EU MDR Lead Auditor Training will provide learners with the knowledge and skills required to lead audits of medical device quality management systems (MD-QMS) against the European Union’s Medical Device Regulation (EU MDR 2017/745) in accordance with ISO 19011 and ISO 17021 as applicable.

Post Market Surveillance (PMS) under EU MDR 2017/745 for Practitioners
4.4 ★★★★★ 13 Reviews
EU MDR Post Market Surveillance Medical Devices

Post Market Surveillance (PMS) Practitioner

14hrs
RAPS Certified Course
Price: $1195.00

Post Market Surveillance (PMS) Training is for those looking to master the post market surveillance requirements under the EU MDR 2017/745

ISO 13485 + EU MDR Internal Auditor Training
4.3 ★★★★★ 6 Reviews
ISO 13485 EU MDR Medical Devices

ISO 13485 + EU MDR Internal Auditor Training

24hrs
CQI-IRCA Certified Course
Price: $1495.00

ISO 13485 and EU MDR Internal Auditor Training is for anyone that wants to be part of the team that performs internal audits of part of their Quality Management System (QMS) based on ISO 13485, including the additional requirements under EU MDR 2017/745, in accordance with ISO 19011.

Person Responsible for Regulatory Compliance (PRRC) Training
4.6 ★★★★★ 33 Reviews
EU MDR EU IVDR PRRC Medical Devices

Person Responsible for Regulatory Compliance (PRRC) Training

6hrs
RAPS Certified Course
Price: $695.00

Person Responsible for Regulatory Compliance (PRRC) Training provides clarity on the role and responsibilities of the PRRC introduced under Article 15 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).

Post Market Surveillance (PMS) Requirements Training
4.5 ★★★★★ 6 Reviews
EU MDR Post Market Surveillance Medical Devices

Post Market Surveillance (PMS) Requirements Training

6hrs
RAPS Certified Course
Price: $695.00

Post Market Surveillance (PMS) Requirements Training is for those looking to understand the fundamentals of post market surveillance requirements under the EU MDR 2017/745

Introduction to EU MDR 2017/745 Training
4.6 ★★★★★ 202 Reviews
EU MDR Medical Devices

Introduction to EU MDR 2017/745

45mins

Introduction to EU MDR Training is for organizations looking for a concise, high-level introduction for their staff.

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  • Trusted By Notified Bodies & Global Brands
  • Trusted By Notified Bodies & Global Brands
  • Trusted By Notified Bodies & Global Brands
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2026 Training Guide

Transformational Training for ISO Standards, Auditing & Medtech QA/RA

2026 Training Guide

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Our team has you covered with expert insights & updates to stay on top of the latest updates, trends, and changes in the industry.

Design Controls, Design and Development under FDA QMSR
Design Controls, Design and Development under FDA QMSR
Michelle discusses Design Controls, ISO 13485 Design and Development and what endures under the FDA's QMSR in effect from February 2026....
Reaffirmed, Not Static: ISO 13485 and the Global Regulatory Evolution
Reaffirmed, Not Static: ISO 13485 and the Global Regulatory Evolution
Michelle discusses the recent affirmation of ISO 13485:2016 and shares her insights on the new guidance reflecting a Global Regulatory Evolution....
Low Risk Does Not Mean No Risk
Low Risk Does Not Mean No Risk
Michelle discusses why ISO 13485 and ISO 14971 make a critical clarification on Risk, and clarifies a dangerous misconception in medical device develo...

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