Do you provide the EMVS Master Data Guide as download?
Why aren't all countries listed in appendix 4 of the Master Data Guide?
Does the strength and pharmaceutical form need to be added to the Registered Product Name to form the Name of the Medicinal Product?
EU HUB | Why are some fields becoming mandatory, and what is the background
behind their implementation?
EU HUB | When will the new mandatory fields be introduced in the Product Master
Data and Product Pack Data?
EU HUB | Are there any changes to the interface that I should be aware of? If yes,
what should I do and how will I be affected?
EU HUB | What are the new mandatory fields?
EU HUB | Do we have to update the already uploaded Product Master Data and Product
Pack Data?
EU HUB | How can I update existing Product Master Data (PMD)?
EU HUB | Is there a deadline by which I should update the Product Master Data and
Product Pack Data?
EU HUB | Are there any consequences of not updating the Product Master Data and Product Pack Data?
EU HUB | How to Fulfill Product Master Data and Batch Data for the EU Hub
EU HUB | Batch Recall Transaction
New Version of Product Master Data (PMD) Guide Released
EU Hub Release 1.16 Error Messages
[EU-HUB] - Release 1.16 - Mandatory Fields PMD & PPD Update
What does it mean when one or more fields of the Product Master Data uploaded by my OBP have been identified as ‘Incorrect’ by EMVO?
Why does the EMVS community need good data quality in the Product Master Data uploaded in the EU Hub?