Online & Blended Medical Devices Quality/Regulatory Training Courses

Introducing industry-leading online, virtual & blended ISO 13485, EU MDR, ISO 14971 plus more Quality & Regulatory Affairs training courses, the likes of which you have never seen before!

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Comply Guru are proudly offering CQI & IRCA and Exemplar Global Approved Online, Blended & Virtual Classroom Training Courses.
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Online & Blended Medical Devices Quality/Regulatory Training Courses

Comply Guru™ is offering online, virtual & blended Medical Devices (Quality Assurance & Regulatory Affairs) Training Courses including ISO 13485:2016, EU Medical Device Regulation (MDR), Risk & ISO 14971:2019, MD SAP & more.

ISO 13485:2016 is a Quality Management System Standard which outlines the requirements for regulatory purposes. These requirements are intended to be applicable to any medical device organisation regardless of size and activity as a basis for demonstrating and supporting compliance with applicable regulatory requirements.

The European Medical Device Regulation (MDR) is a set of regulations that must be met if producing or distributing medical devices within the EU, and if you want to sell your Medical Devices in the EU. Comply Guru have partnered with Meddev Solutions UK to develop online & self-paced courses on the EU MDR which are now available!

Request a free demo today to see if our training is for you!

Watch our video for Online & Blended Medical Devices Quality/Regulatory Training Courses

This video is some of the highlights from a Q&A Session with Eoin P. Kelly, Founder & CEO of Comply Guru, regarding the big vision for Comply Guru; various topics & whats in the pipeline for 2020!

    Available Courses

  • Online & Self-Paced Basic Overview of EU Medical Device Regulation (MDR 2017/745) Course

    ★★★★★ (62 Reviews, Click to view)

    Language: English

    Our online, self-paced course is aimed at anyone working in the medical device industry sector who is looking for a general overview of the EU MDR. + View More

    Duration :2hrs

  • Online & Self-Paced ISO 13485:2016 Foundation Course (CQI & IRCA Certified)

    ★★★★★ (29 Reviews, Click to view)

    Language: English

    A CQI & IRCA Certified online & self-paced course for anyone looking to gain a comprehensive understanding of the core requirements of ISO + View More

    Duration :8hrs

  • Online Comprehensive EU Medical Device Regulation (MDR) 2017/745 Practitioner Course | Exemplar Global Certified

    ★★★★★ (17 Reviews, Click to view)

    Language: English

    Our Exemplar Global Certified online, self-paced Comprehensive EU Medical Device Regulation (MDR) 2017/745 Practitioner Course can take you through + View More

    Duration :20hrs

  • Online & Blended ISO 13485:2016 Internal Auditor Training (CQI & IRCA Certified)

    ★★★★★ (18 Reviews, Click to view)

    Language: English

    This CQI & IRCA Certified blended course (online & classroom/virtual training) is ideal for anyone that has a good understanding of Quality + View More

    Duration :16hrs

  • Online & Blended ISO 13485:2016 Lead Auditor Training (CQI & IRCA Certified)

    ★★★★★ (58 Reviews, Click to view)

    Language: English

    This CQI & IRCA Certified blended course (online & classroom/virtual training) is ideal for anyone that has a good understanding of Quality + View More

    Duration :40hrs

  • Online & Self-Paced Risk Management & ISO 14971:2019 Training Course

    ★★★★★

    Language: English

    This online, self-paced course will offer an interactive, comprehensive overview of risk management to medical devices based on ISO 14971:2019 whic + View More

    Duration :8hrs Release Date :17th March 2021

  • Upcoming Courses

  • Online & Self-Paced Comprehensive EU In-Vitro Diagnostic Regulation (IVDR) 2017/746 Practitioner Course

    ★★★★★

    Language: English

    Our online, self paced course provides an in-depth foundation on the key principles and practices required for the new European In-Vitro Diagnostic + View More

    Duration :18hrs

  • EU Medical Device Regulation 2017/745 Auditor (EU MDR) Training

    ★★★★★

    Language: English

    The aim of this course is to provide learners with the knowledge and skills required to perform  third-party audits of medical device quality mana + View More

    Duration :24hrs

  • Online & Self-Paced Medical Device Single Audit Program (MDSAP) Foundation Course

    ★★★★★

    Language: English

    Our online interactive course provides a comprehensive Foundation on the Medical Device Single Audit + View More

    Duration :8hrs

  • Medical Device Single Audit Program (MDSAP) Auditor Training

    ★★★★★

    Language: English

    The aim of this course is to provide learners with an appreciation or the knowledge and skills required to complete an audit against the IMDRF Medi + View More

    Duration :16hrs

  • Online & Self-Paced U.S. FDA Quality Systems Regulation (QSR) 21 CFR 820 Course

    ★★★★★

    Language: English

    This online, interactive course will provide a comprehensive introduction to the U.S Quality Systems Regulation (21 CFR 820).

    Duration :8hrs

  • Online & Self-Paced Clinical Evaluation for Medical Devices Course

    ★★★★★

    Language: English

    This online course will offer an interactive overview of Clinical Evaluation for Medical Devices & MEDDEV 2.7/1.

    Duration :8hrs