Senior Pharmaceutical Technician
I am a member of the technical department of the Pharmaceutical Technical Cabinet M. Camps since 2007, Bachelor of Pharmacy from the University of Barcelona in 1995, I currently have an extensive professional career advising companies in the pharmaceutical, health and cosmetic sectors. I am responsible for the area of medical device and elaboration of tecnichal file for the application of the CE marking of Medical Devices, complementing my time with projects in the cosmetic field.
Before my incorporation into the GTF my professional experience was developed in the pharmaceutical inspection of medicinal goods (border controls) and previously in a laboratory of raw materials, pharmaceuticals and cosmetics.
Single identification of the product: What will be possible with the new UDI system for Medical Devices?
In April 2013, the European Commission issued a recommendation concerning a common framework for a single identification system for medical devices in the EU. This was intended to lay the foundations for the EU's future identification and traceability infrastructure, in line with the latest developments worldwide.
Since then, the European Commission has promoted, through the publication of Article 26 of Regulation (EU) 2017/745 on Medical Devices, and Article 23 of Regulation (EU) 2017/746 on Medical Devices for In-Vitro Diagnostics, two essential initiatives aimed at providing coverage to the UDI system:
- The creation of the Medical Devices database Eudamed (whose name is an acronym for European Database on Medical Devices).
- The creation of the European Medical Device Nomenclature (EMDN) body, which provides support and facilitates the creation of the Eudamed database.
UDI: Identification that is primarily aimed at the safety of EU consumers
In short, the new Unique Device Identifier system – UDI will facilitate the traceability of medical devices. In parallel, post-market activities relating to product safety will also be stronger and will allow better monitoring by the competent authorities.
In addition, the European Commission, using EMDN, has created a FAQ document relating to the Unique Device Identifier – UDI. Read her now!
Unique Device Identifier (UDI) in Medical Devices
Click at the link to visit the European Commission’s Unique Device Identifier – UDI website, where you will find all the information about the European Medical Device Nomenclature (EMDN) initiative and Eudamed, the new European Medical Device'sDatabase.
This web portal, created by the European Commission, is a space that will allow you to know, at first hand, all the official information from the health authorities in the euro area and all the new developments in relation to the new Unique Device Identifier - UDI and its implementation process.