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:
a. The regulatory background to IDMP
b. Definition of IDMP
c. Understanding the key terms within IDMP
d. Impact of IDMP on other divisions of your organization
e. IDMP implementation Challenges
f. Logical approach to IDMP
g. Penalties of non-compliance to IDMP
h. Benefits of implementing IDMP for your organization