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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Online & Self-Paced Comprehensive EU In-Vitro Diagnostic Regulation (EU-IVDR 2017/746) Practitioner Course★★★★★
Our online, self paced course provides an in-depth foundation on the key principles and practices required for the new European In-Vitro Diagnostic + View More
Duration :18hrs Release Date :1st September 2021
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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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