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!

Some Companies that have used Comply Guru™

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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

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