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!
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- ★★★★★ (113 Reviews, Click to view)
Our online, self-paced course is aimed at anyone working in the medical device industry sector who is looking for a basic overview of the EU MDR 20 + View More
Duration :2hrs Continuing Education Units :0.2
Online Comprehensive EU Medical Device Regulation/MDR 2017/745 Practitioner Course | CQI, IRCA & Exemplar Global Certified★★★★★ (53 Reviews, Click to view)
Our online, self-paced CQI, IRCA & Exemplar Global certified comprehensive EU MDR 2017/745 Practitioner course can take you through the regulat + View More
Duration :20hrs Continuing Education Units :2.0
The aim of this course is to provide learners with the knowledge and skills required to perform third-party audits of medical device quality mana + View More
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Gave us 4/5 Stars or higher Overall Training Experience
Would Recommend Online or Blended Training over Classroom Training
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