en English
ar Arabicbg Bulgariancs Czechen Englishfr Frenchde Germanel Greekit Italianpl Polishru Russianes Spanishuk Ukrainian
mobile-logo
worldwide UDI requirements for medical devices
29 Sep

[Whitepaper] Medical devices: Overview UDI Requirements worldwide

by Milena Atanasova
in news, Whitepapers
Comments

 

Learn everything about the new EU requirements to medical devices regarding MDR.

 

 

Download the whitepaper now by filling the fields below and learn about the UDI requirements around the world.

 

 

 

 

 



    I have read the Privacy policy and confirm my willingness to receive marketing materials and updates from SoftGroup.

    More Resources

    Medical devices in UK market after brexit
    [Blog] Medical Devices access to UK market after the Brexit
    mdr questions
    [Whitepaper] Frequently Asked Questions About Medical Devices
    webinar key aspects of mdr
    [Webinar]: Key aspects of EU regulation regarding the medical devices by GS1 and SoftGroup
    [Webinar]: The backup plan for serialization
    Pharma Serialization, Aggregation and Track and Trace Software by SoftGroup Top

    By continuing to use the site, you agree to the terms of our Privacy and Cookies Policy and the use of cookies. Privacy and Cookies Policy

    The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.

    Close