HUG Information Day 2017 on FMD and UDI

Safer More Efficient Care Starts with a Simple Scan

Getting ready for the EU Pharmaceutical and Medical Device Regulations – Implications for Hospitals and Suppliers

Event held Tuesday 28th March 2017 in Cherry Orchard Hospital, Dublin. We would like to extend a big thank you to all our speakers and supporters including the HSE, HPRA, IMVO, GS1 Global, Hospitals and Suppliers.

Morning Session: Falsified Medicines Directive

The morning session focussed on the Falsified Medicines Directive (FMD). The EU date for compliance is 19th Feb 2019.

Session Chair: Orlaith Brennan, IPHA

Speakers and Presentations

(Please click on the presentation you would like to download. The pdf will open in a new window.)

Afternoon Session: Medical Device Regulation - Unique Device Identification

The afternoon session focussed on the Medical Devices Regulation (MDR) and Unique Device Identification (UDI). The EU date for compliance is 2020.

Session Chair: John Swords, HSE

Speakers and Presentations

(Please click on the presentation you would like to download. The pdf will open in a new window.)

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Giving time back to patient care

The initiative provides traceability of items used during surgery and procedures, improving the standard of care provided to patients and the Hospital's efficiency.

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