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.

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

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    Available Courses

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

    ★★★★★ (246 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)

    ★★★★★ (326 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 (EU-MDR 2017/745) Practitioner Course | CQI, IRCA & Exemplar Global Certified

    ★★★★★ (171 Reviews, Click to view)

    Language: English

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

    Duration :20hrs

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

    ★★★★★ (127 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 :24hrs

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

    ★★★★★ (201 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 :48hrs

  • Online & Self-Paced Risk Management & ISO 14971:2019 Training Course (CQI, IRCA & Exemplar Global Certified)

    ★★★★★ (224 Reviews, Click to view)

    Language: English

    This CQI, IRCA & Exemplar Global Certified Online, Self-Paced Medical Device Risk Management based on ISO 14971:2019 Training Course will offer + View More

    Duration :8hrs

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

    ★★★★★ (16 Reviews, Click to view)

    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

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

    ★★★★★

    Language: English

    Our Exemplar Global Certified Online & Self-Paced Course aims to provide learners with the knowledge required to understand the IMDRF Medical D + View More

    Duration :8hrs

  • Upcoming Courses

  • Online & Self-Paced FDA QSR 21 CFR 820 + ISO 13485:2016 Course

    ★★★★★

    Language: English

    Our self-paced, interactive course will provide each Learner with a solid Foundation on both the FDA Quality Systems Regulation (21 CFR 820) and IS + View More

    Duration :12hrs Release Date :1st July 2022

  • 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

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The Numbers - How We Are Doing

  • 100%

    Our Pass Rate

  • 100%

    Would Recommend Comply Guru

  • 97%

    Gave us 4/5 Stars or higher Overall Training Experience

  • 96%

    Would Recommend Online or Blended Training over Classroom Training

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