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!
Request a free demo today to see if our training is for you!
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Online & Self-Paced ISO 13485:2016 Foundation Course (CQI & IRCA Certified)
★★★★★ (36 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 & Self-Paced Basic Overview of EU Medical Device Regulation (MDR 2017/745) Course
★★★★★ (71 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 Comprehensive EU Medical Device Regulation (EU-MDR 2017/745) Practitioner Course | CQI, IRCA & Exemplar Global Certified
★★★★★ (27 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)
★★★★★ (29 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 :16hrs
Online & Blended ISO 13485:2016 Lead Auditor Training (CQI & IRCA Certified)
★★★★★ (81 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 :40hrs
Online & Self-Paced Risk Management & ISO 14971:2019 Training Course
★★★★★Language: English
This online, self-paced course will offer an interactive, comprehensive overview of risk management to medical devices based on ISO 14971:2019 whic + View More
Duration :8hrs Release Date :17th March 2021
Online & Self-Paced Comprehensive EU In-Vitro Diagnostic Regulation (EU-IVDR 2017/746) Practitioner Course
★★★★★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 Release Date :17th May 2021
Upcoming Courses
EU Medical Device Regulation 2017/745 Auditor (EU MDR) Training
★★★★★Language: English
The aim of this course is to provide learners with the knowledge and skills required to perform third-party audits of medical device quality mana + View More
Duration :24hrs
Online & Self-Paced Medical Device Single Audit Program (MDSAP) Foundation Course
★★★★★Language: English
Our online interactive course provides a comprehensive Foundation on the Medical Device Single Audit + View More
Duration :8hrs
Medical Device Single Audit Program (MDSAP) Auditor Training
★★★★★Language: English
The aim of this course is to provide learners with an appreciation or the knowledge and skills required to complete an audit against the IMDRF Medi + View More
Duration :16hrs
Online & Self-Paced U.S. FDA Quality Systems Regulation (QSR) 21 CFR 820 Course
★★★★★Language: English
This online, interactive course will provide a comprehensive introduction to the U.S Quality Systems Regulation (21 CFR 820).
Duration :8hrs
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
- 100%
Our Pass Rate
- 100%
Would Recommend Comply Guru
- 97%
Gave us 4/5 Stars or higher Overall Training Experience
- 96%
Would Recommend Online or Blended Training over Classroom Training
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