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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- ★★★★★ (62 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
Online Comprehensive EU Medical Device Regulation/MDR 2017/745 Practitioner Course | Exemplar Global Certified★★★★★ (17 Reviews, Click to view)
Our online, self-paced Exemplar Global certified comprehensive EU MDR 2017/745 Practitioner course can take you through the regulation, not just fr + View More
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