Avery Dennison over Richtlijn vervalste geneesmiddelen

The EU Directive on Falsified Medicines (Directive 2011/62/EU) was published in July 2011. It reflects an increasingly complex distribution network for medicinal products, with many different players – and a pressing need to ensure reliability across the entire supply chain.
Harmonized safety features across the entire EU are on their way. Legislation will be in force by the end of 2015, and manufacturers and other stakeholders will then have three years to decide on and implement a range of different safety features. It means new responsibilities for wholesalers and brokers, including logos for legally operating online pharmacies (Labels & Labelling, 4 augustus 2015).
Klik hier om de white paper te downloaden (764 kB).
Klik hier voor meer informatie over de NVC E-Course Pharmaceutical Packaging.
Klik hier voor informatie over de farmaceutische verpakkingsbeurs InnoPack 2015 (Madrid, 13-15 oktober).

Heeft u vragen over dit onderwerp, neem dan contact met ons op via e-mail of bel: +31-(0)182-512411. Dit bericht is ook opgenomen in ons maandelijkse overzicht, de NVC Members-only Update.