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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Online & Self-Paced Medical Device Single Audit Program (MDSAP) Foundation Course | Exemplar Global Certified★★★★★
Our self-paced course provides an introduction to the Medical Device Single Audit Program (MD + View More
Duration :8hrs CEUs :0.8 Release Date :17th March 2022 Continuing Education Units :0.8
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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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