News & Events

EU FMD - Preparing for Compliance

By aisltd, Monday, 30th May 2016 | 0 comments
Filed under: Industry News.

With the publication of the Delegated Act on safety features, those who manufacture, sell, or dispense medications in the European Union (EU) have until February 2019 to comply with complex new track-and-trace regulations outlined in the Falsified Medicines Directive (FMD).

Click here to read a useful summary article.

The legislation also states that all medicines must have a 'tamper evident' safety feature.  One of our partners, Herma, the world's leading manufacturer of labelling machines, have a new machine specially designed to apply TE labels to medicinal products. More information is available here

Should you wish to speak to one of our experts on what this legislation means for your production line, please call us or email info@aisltd.ie 

 



Dublin

Automatic Identification Systems Ltd

Cork

Automatic Identification Systems Ltd
Unit 35 Eastgate Drive,
Little Island, Cork,  
T45 C925, Ireland

Phone: +353 (0)21 235540
Fax: +353 (0)1 6205735
Email: info@aisltd.ie

Barcelona

AIS Vision Systems S.L
Pol. Ind. Can Roqueta,
Avda. Can Bordoll, 119 Sabadell,
Barcelona 08202, Spain

Phone: +34 931 003 035
Fax: +34 931 003 038
www.aisvision.com

Beugen

AIS-Scanology B.V. 
Laan de Wijze 20,
5835 DS Beugen
The Netherlands

Phone: +31 (0)485-561616
Fax: +31 (0)485-561610
www.scanology.nl

 

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