Electronic Data Interchange (EDI)
With a web solution, WebEDI in short, the supplier receives the orders on a website that is not connected to their internal system. The supplier also enters the delivery note and invoice on the same website.
This solution does require manual...
My recipient can’t see my products
You can use the following checklist to make sure that everything is correct:
Product images and digital assets
Filling in the packaging information about packaging - examples DIY, garden & pet
Example 1: Lamp - Example 2: Roller blind - Example 3: Primer - Example 4: Cat milk - Example 5: Wet food for cat
Attention! The chosen values are illustrative and can vary from the real values..
- Only for the main packaging element, you select a...
The renewed audit programme: a boost for your data quality!
Additionally, we are expanding the programme to new product categories. In addition to pre-packaged food, we will now audit detergents, cosmetics, and pet food.
Collaboration with the industry
The renewed audit programme is the result of extensive...
US legislation Food and Drug Administration (FDA)
The US FDA introduced this regulation in September 2013 to create a global, unique system for the identification of all medical devices sold in the United States. The US FDA wants to ensure patient safety and better protect the supply chain in the healthcare sector with this regulation.
Suppliers of medicines
Combating counterfeit medicines
The FMD does this for both prescription and non-prescription medication.
Need for more efficiency in logistics
From the electronic processing of the order and delivery to the invoice.
GS1 standards contribute to increased efficiency and thus protect the five rights of the patient:
"The right dose of the right medication to the right person at the right time and in the right way."
FAQ My Basic UDI-DI Manager
Here you can find the most frequently asked questions on My Basic UDI-DI Manager.