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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- ★★★★★ (227 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★★★★★ (129 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
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