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.
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Online & Self-Paced Risk Management & ISO 14971:2019 Training Course (CQI, IRCA & Exemplar Global Certified)★★★★★ (224 Reviews, Click to view)
This CQI, IRCA & Exemplar Global Certified Online, Self-Paced Medical Device Risk Management based on ISO 14971:2019 Training Course will offer + View More
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