The third party submitter is not authorized to subm

[bcotton56]

Where in the app do i put my 3rd party (1world)  No matter where I put the info I get the c999 error.

[bcotton56]

My gudid account lists 1world as the 3rd party.  I have key's duns listed as brand owner additional info, 1world duns as additional trade item identification.  Where should I have Key's duns listed and where for 1worlds?

[bcotton56]

My gudid account lists 1world  as third party.  I do NOT need another account.  If you look at production items, there are several places asking for duns numbers.  Nothing I can find tells me which duns goes in which spot.  That's what I need help with now.

[DanV]

Hi bcotton56

Use your Duns number in Item Management for attribute Brand Owner Additional Trade Item Identification Value:

[bcotton56]

I have my duns number listed there now and item synced.  Nowhere in by product lists 1world duns.  Am I missing something?

[DanV]

Hi bcotton56,

Looks like you did submit the FDA UDI form with the 1WS Duns number that allows 1WS to send your items to the FDA on your behalf. If you received a Synchronized CIC back from the FDA you should be all set with that item.

TIP: Any items that were Synchronized in the Pre-Production environment can be extracted from Item Management Pre-Prod, on the FUSE extract set the Operation to ADD and Import Item to Y, then you can upload that FUSE extract in Production Item Management to create your item with all the attribute values you that are present in Pre-Prod.

[bcotton56]

When will I be able to see my product in accessgudid

[DanV]

Hi bcotton56, 

I dont see anything in the FDA Implementation Guide about any timing between the Synchronized CIC from the FDA and when your item will show in accessgudid, it simply states the below:

The process is complete when the CIC state of SYNCHRONIZED has been
received for all of the published items.

If you have not done so already please check for your item in accessgudid, if it is not present there, I would recommend reaching out to the FDA.