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 Basic Overview of EU Medical Device Regulation (MDR 2017/745) Course
★★★★★ (246 Reviews, Click to view)Language: English
Our online, self-paced course is aimed at anyone working in the medical device industry sector who is looking for a general overview of the EU MDR. + View More
Duration :2hrs
Online & Self-Paced ISO 13485:2016 Foundation Course (CQI & IRCA Certified)
★★★★★ (326 Reviews, Click to view)Language: English
A CQI & IRCA Certified online & self-paced course for anyone looking to gain a comprehensive understanding of the core requirements of ISO + View More
Duration :8hrs
Online Comprehensive EU Medical Device Regulation (EU-MDR 2017/745) Practitioner Course | CQI, IRCA & Exemplar Global Certified
★★★★★ (171 Reviews, Click to view)Language: English
Our CQI, IRCA & Exemplar Global Certified online, self-paced Comprehensive EU Medical Device Regulation (MDR) 2017/745 Practitioner Course can + View More
Duration :20hrs
Online & Blended ISO 13485:2016 Internal Auditor Training (CQI & IRCA Certified)
★★★★★ (127 Reviews, Click to view)Language: English
This CQI & IRCA Certified blended course (online & classroom/virtual training) is ideal for anyone that has a good understanding of Quality + View More
Duration :24hrs
Online & Blended ISO 13485:2016 Lead Auditor Training (CQI & IRCA Certified)
★★★★★ (201 Reviews, Click to view)Language: English
This CQI & IRCA Certified blended course (online & classroom/virtual training) is ideal for anyone that has a good understanding of Quality + View More
Duration :48hrs
Online & Self-Paced Risk Management & ISO 14971:2019 Training Course (CQI, IRCA & Exemplar Global Certified)
★★★★★ (224 Reviews, Click to view)Language: English
This CQI, IRCA & Exemplar Global Certified Online, Self-Paced Medical Device Risk Management based on ISO 14971:2019 Training Course will offer + View More
Duration :8hrs
Online & Self-Paced Comprehensive EU In-Vitro Diagnostic Regulation (EU-IVDR 2017/746) Practitioner Course
★★★★★ (16 Reviews, Click to view)Language: English
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
Online & Self-Paced Medical Device Single Audit Program (MDSAP) Foundation Course | Exemplar Global Certified
★★★★★Language: English
Our Exemplar Global Certified Online & Self-Paced Course aims to provide learners with the knowledge required to understand the IMDRF Medical D + View More
Duration :8hrs
Upcoming Courses
Online & Self-Paced FDA QSR 21 CFR 820 + ISO 13485:2016 Course
★★★★★Language: English
Our self-paced, interactive course will provide each Learner with a solid Foundation on both the FDA Quality Systems Regulation (21 CFR 820) and IS + View More
Duration :12hrs Release Date :1st July 2022
Online & Self-Paced Clinical Evaluation for Medical Devices Course
★★★★★Language: English
This online course will offer an interactive overview of Clinical Evaluation for Medical Devices & MEDDEV 2.7/1.
Duration :8hrs
Some Companies that have used Comply Guru™
The Numbers - How We Are Doing
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100%
Our Pass Rate
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100%
Would Recommend Comply Guru
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97%
Gave us 4/5 Stars or higher Overall Training Experience
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96%
Would Recommend Online or Blended Training over Classroom Training
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