Online & Blended Medical Devices Quality/Regulatory Training Courses

Introducing industry-leading On-Demand (24/7)  ISO 13485, ISO 14971, EU-MDR 2017/745, EU-IVDR 2017/746, MDSAP, FDA QSR 21 CFR Part 820 plus more Quality & Regulatory Affairs training courses, the likes of which you have never seen before!

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

Gain a sneak peek at Comply Guru’s industry-leading methodology & approach for truly online learning!

    Upcoming Courses

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

    ★★★★★ ( Reviews, Click to view)

    Language: English

    This online course will offer an interactive overview of Clinical Data 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

  • 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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