June 26, 2024

In Vitro Diagnostic Medical Device Regulation (IVDR) Postgraduate Training

Are you ready to take your understanding of In Vitro Diagnostic Medical Device Regulation (IVDR) to new heights?

Are you interested in becoming a highly skilled auditor, product assessor or clinical reviewer against the EU In Vitro Diagnostic Medical Device Regulation (IVDR)?

Registrations are NOW OPEN for our postgraduate course: Generating Data for Technical Documentation (IVDR)!

This comprehensive module offers a deep dive into the construction of the Technical Documentation and the Clinical Evaluation Report, building on the foundational knowledge from Module 1.

Course Details:

Start Date: October 7th, 2024

Application Period: June 24th – August 30th, 2024

Course Format:

Duration: 10 weeks (8 weeks in the virtual classroom + 2 weeks for online assessments)

Delivery Mode: 100% online


Postgraduate CPD certificate worth 5 credits

Accredited by Technological University Dublin (TU Dublin)

Dr. Geofrey De Visscher, Head of SGS’s European MDR Notified Body (NB)

Final Award:

CPD certificate in Generating Data for Technical Documentation (IVDR)

Awarded at NFQ IRL Level 9 and EQF Level 7 without classification, accredited by TU Dublin

Don’t let this opportunity pass you by! Step up and make a meaningful impact on the safety and effectiveness of Medical Devices in the market. Elevate your expertise, embrace the future of IVDR, and join us on this exciting journey of learning and progress.

REGISTER NOW and be a frontrunner in Medical Device Regulation!

Click on the link below to secure your spot in the IVDR Masters-Level Module today!


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