Sign for Notice Everyday    Sign Up| Sign In| Link| English|

Our Sponsors

    Receive Latest News

    Feedburner
    Share Us

    Implementing UDI (Unique Device Identification) - Plan Now for Success

    View: 47

    Website https://www.complianceonline.com/medical-device-udi-implementation-seminar-training-80303SEM-prdsm?c | Want to Edit it Edit Freely

    Category

    Deadline: March 06, 2021 | Date: March 16, 2021

    Venue/Country: U.S.A

    Updated: 2021-02-06 17:20:27 (GMT+9)

    Call For Papers - CFP

    The one-day virtual seminar provides the information you need to implement UDI. An effective implementation gives your customers the information they need. It will also help you avoid an FDA 483 and a Warning Letter.

    The virtual seminar gives you hands on experience to understand UDI and your device. You bring a laptop computer and some information about your device. During the seminar you receive toolkits to determine the compliance dates, packaging configurations, and the attributes you will load to GUDID

    The seminar helps you identify the requirements for the UDI elements:

    Procedure changes

    Label UDI

    Package UDI

    Direct marking UDI

    Date format

    Entry into GUDID

    The seminar helps you implement the changes, update your procedures, and determine when you need to revalidate databases.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.