Uploading of newly authorised products

When a new product receives authorisation through the Centralised Procedure, I can see the product name in the list of products for my company.
However, there are no records for display.
Does the EMA do anything post authorisation, or is it up to the MAH to upload a complete set of "blank" records - all licenses for all countries - with the Marketing Status of "Not marketed"?  Then each country affilaite can update its records when they commence marketing of the new product in their country.

Have you received any answer on this question?

Please consult the specific EMA page, Notifying a change of marketing status | European Medicines Agency (europa.eu), which reports the obligations of the Marketing Authorization holders and the procedure to fulfil them.