Online & Blended Medical Devices Quality/Regulatory Training Courses
Comply Guruâ„¢ 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!
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Online & Self-Paced Risk Management & ISO 14971:2019 Training Course (CQI, IRCA & Exemplar Global Certified)
★★★★★ (38 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
Available Courses
Some Companies that have used Comply Guruâ„¢
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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