Online & Blended Medical Devices (Quality and 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.

Online & Blended Medical Devices (Quality and 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 and 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

    ★★★★★ (42 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)

    ★★★★★ (18 Reviews, Click to view)

    Language: English

    A CQI & IRCA Certified self-paced course for anyone looking to gain a comprehensive understanding of the core requirements of ISO 13485:2016.+ View More

    Duration :8hrs

  • Online & Self-Paced EU Medical Device Regulation (MDR 2017/745) In-Depth Foundation Course

    ★★★★★ (1 Reviews, Click to view)

    Language: English

    Our online, self-paced Exemplar Global certified comprehensive EU MDR course can take you through the regulation, not just from an industry perspec + View More

    Duration :20hrs

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

    ★★★★★ (50 Reviews, Click to view)

    Language: English

    This CQI & IRCA Certified blended course (online, self-paced & virtual classroom) is ideal for anyone that has a good understanding of Qual + View More

    Duration :45hrs

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

    ★★★★★ (13 Reviews, Click to view)

    Language: English

    This CQI & IRCA Certified blended course (online, self-paced & virtual classroom) is ideal for anyone that has a good understanding of Qual + View More

    Duration :16hrs

  • Upcoming Courses

  • Online & Self-Paced Risk Management & ISO 14971:2019 [including Key Changes] Training Course

    ★★★★★

    Language: English

    This online course will offer an interactive, comprehensive overview of risk management to medical devices based on ISO 14971:2019 which has just b + View More

    Duration :8hrs

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

    ★★★★★

    Language: English

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

    Duration :8hrs

  • 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 :16hrs

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

    ★★★★★

    Language: English

    Our online interactive course provides an introduction to the Medical Device Single Audit Pro + View More

    Duration :8hrs

  • Online & Self-Paced In Vitro Diagnostic Medical Devices Regulation (IVDR) In-Depth Foundation Course

    ★★★★★

    Language: English

    Our online interactive course provides an in-depth foundation on the application of the key principles and practices required for the new In Vitro + View More

    Duration :8hrs

  • Online Auditing Competency based on ISO 19011:2018 Training

    ★★★★★

    Language: English

    This course is ideal for anyone that needs to conduct an audit of an organizations ISO based management system (For example: ISO 9001, ISO 14001, I + View More

    Duration :7hrs

Some Companies that have used Comply Guru™

The Numbers - How We Are Doing

  • 100%

    Our Pass Rate

  • 100%

    Would Recommend Comply Guru

  • 99%

    Gave us 4/5 Stars or higher Overall Training Experience

  • 95%

    Would Recommend Online or Blended Training over Classroom Training

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