UDI – Anforderungen an Medizinprodukte und In-vitro-Diagnostika

Ein Gemeinschaftsseminar mit der DIN-Akademie. Berlin

http://www.beuth.de/de/seminar/udi-anforderungen-an-medizinprodukte-und-in-vitro-diagnostika/271142095

Manafactures managing UDI

The labeling requirement for medical devices in the US and EU with the UDI system expands.

After the date September 24, 2016 for the registration of medical devices in the US Class II in the "Global UDI Data Base - GUDID it goes according to the plan of the FDA in the phase of the last group of Class I.

The new EU regulation for medical devices "Medical Device Regulation (MDR)" is now at the start as part of "UDI".

For information about the UDI implementation steps in accordance with the identification and registration requirements for UDI in USA and Europe and how manufacturers UDI manage, you can log in to the following event dates:

Date	Host	Information	Registration	Program
17th of May, 2017	Med+Logistica, Leipzig, Germany	healthcaretag.de	Thank you for your participation.
Past events
24th November, 2016	Hilton Metropole, London, UK		Thank you for your participation.
29th November, 2017	Medical-Mountains AG Tuttlingen Germany		Thank you for your participation.
26th of September, 2016	IHK Darmstadt, Germany		Thank you for your participation. Resources are online.
28th of September, 2016	Medical-Valley Erlangen, Germany		Thank you for your participation. Resources are online.