Etiketteervoorschriften EU MDR: Leren van ervaringen met UDI

The European medical device industry is in the grip of the biggest changes the market has seen in decades: the European Medical Device Regulation. These new rules to ensure the safety of medical devices became active in June 2017, imposing major new requirements on anybody involved in the design, manufacture, approval and commercialization of devices that are sold in the EU.
The final directive aims to establish a robust, transparent, predictable and sustainable regulatory framework allowing the ability to trace a device from its manufacturer through the supply chain to the final end user. This whitepaper shows the significant ramifications the regulation will have on labelling operations.
Klik hier om de whitepaper EU MDR Labeling Compliance: Learning the Lessons from UDI van PRISYM ID en Be4Ward te downloaden (registratie verplicht).
Klik hier voor meer informatie over het NVC-project Pharmaceutical Packaging Innovation.
Klik hier voor meer informatie over de Live Online NVC E-Course Pharmaceutical Packaging.

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