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 (EU-MDR), Risk & ISO 14971:2019, MDSAP & 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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Gain a sneak peek at Comply Guru’s industry-leading methodology & approach for truly online learning!

    Upcoming Courses

  • 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 Continuing Education Units :0.8

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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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