21. marec 2023

    Bela knjiga

    Ne zamudite novega roka EU za MDR

    Does Your Labeling and Artwork Offer a Path to Compliance?

    In February 2023 the European Parliament recognized the critical need to mitigate the risk of shortages for patient safety by granting an extension for the new EU MDR to 2027 or 2028 depending on device’s risk class.

    This passage means medical device manufacturers can now take advantage of this opportunity to properly and cost-effectively implement labeling solutions that offer a clear corridor to compliance.

    Download the whitepaper to learn how to:

    • Avoid recalls and non-compliance
    • Adhere to cross-border regulations 
    • Automate, optimize and centralize labeling
    • Enable fast, flexible label changes
    • Ensure security and auditability

     

    Prenesite in preberite.

    Več izbir ali ena izbira

    Za dodatne podrobnosti glejte Loftwarov pravilnik o zasebnosti

    Za dodatne podrobnosti glejte Loftwarov pravilnik o zasebnosti