Online Medical Device Regulatory Affairs Courses

In partnership with Meddev Solutions, we are offering industry-leading online Medical Device Regulatory Affairs & related training courses, the likes of which you have never seen before!

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Comply Guru are proudly offering CQI and IRCA Approved Online & Virtual Classroom Training Courses.

Online Medical Device Regulatory Affairs Courses

Comply Guru™ are proud to be partnering with Meddev Solutions to design, develop & launch a growing library of Online Medical Device Regulatory Affairs Training Courses!

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Meddev Solutions are a team of QARA professionals, each with a minimum of 20 years’ experience, working in the medical device industry for both manufacturers and Notified Bodies.

They routinely train and provide consultancy services to the top medical device manufacturers & due to their Notified Body experience, they are in an excellent position to ensure our courses deliver knowledge in a meaningful way, that will meet your needs and ensure compliance.

Try our free, online ISO 13485:2016 Introduction course today to see if our online training is the right choice for you!

Watch our video for Online Medical Device Regulatory Affairs Courses

Learn More About Comply Guru's Big Vision

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!

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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

    Premium Courses

  • Online General Overview of EU Medical Device Regulation (MDR) Course

    ★★★★★

    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 EU Medical Device Regulation (MDR) In-Depth Foundation Course

    ★★★★★

    Language: English

    Our online, self-paced comprehensive EU MDR course can take you through the regulation, not just from an industry perspective, but also from a Noti + View More

    Duration :16hrs Release Date :1st July 2020

  • Upcoming Courses

  • Online Clinical Data for Medical Devices and MEDDEV 2.7/1 Course

    ★★★★★

    Language: English

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

    Duration :16hrs

  • Online 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 :16hrs

  • Online 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 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 Regulation Basics for Medical Devices Course

    ★★★★★

    Language: English

    This online course offers an interactive overview of the application of various regulations that apply to medical devices and the various country j + View More

    Duration :2hrs

  • Online Overview of Risk Management & ISO 14971:2019 [including Key Changes]

    ★★★★★

    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

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