Everything you ever wanted to know about IDMP – White Paper
The European Medicines Agency has mandated that organizations doing business in the EU will need to submit product information according to the ISO-IDMP standards by July 2016.
This is however not just a European challenge, as the FDA is working on the adoption of the IDMP standard and it is only a matter of time before this will become mandatory to do business in all key geographies.
This comprehensive whitepaper discusses:
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