Online Medical Device Regulatory Affairs Courses with Meddev Solutions

by Eoin Philip Kelly | December 10, 2019 | Blog , Medical Device Regulatory Affairs , |

Comply Guru is delighted to announce that we are partnering with Meddev Solutions where we will be offering a growing library of Online Medical Device Regulatory Affairs Courses starting in early 2020.

This is the beginning of a very exciting chapter as part of Comply Guru’s strategy to become the leading Platform for Online Compliance-based Training Courses. A key part of that strategy was identifying industry leading experts in their field that we felt were the ‘right fit’ to partner with in offering online highly interactive, highly effective training courses. Meddev ticked all the boxes!

About Meddev Solutions

Meddev Solutions have a highly distinguished reputation both in Ireland & the UK, but also internationally. They are a team of QARA professionals, each with a minimum of 20 years’ experience, working in the medical device industry for both manufacturers and Notified Bodies. Meddev Solutions currently work with all the top medical device manufacturers & due to their Notified Body experience, they are in an excellent position to ensure our online courses deliver the right knowledge in a meaningful way & that it will meet your needs.

What We Will Be Offering

In partnership, our online courses will span across a range of areas starting with Regulation Basics for Medical Devices, EU Medical Device Regulation (MDR), In Vitro Diagnostic Medical Devices Regulation (IVDR), Clinical Data for Medical Devices and MEDDEV 2.7/1, Application of Risk Management & ISO 14971, U.S. FDA Quality System Regulation (QSR) and then growing organically based on the needs of our Customers. We will also be able to cater for any Organization who may be looking for custom training courses in any area of Regulatory Affairs.

For more information about the courses, to download our brochure or to submit your interest, you can visit: https://www.complyguru.ie/online-training/medical-devices-regulatory-courses/

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