Discover our in-depth resources on how to comply with EMA's IDMP regulations.
Helping pharma companies with their IDMP strategy
Identification of Medicinal Products (IDMP) is one of the most significant regulatory challenges for all pharmaceutical companies operating in Europe. How can companies navigate this journey towards increased patient safety and use it as an opportunity for business transformation?
Learn how to have easier and faster access to the correct data to make your IDMP submission and lay the foundation for building a genuinely insight-driven organization.
Find out if you have the best strategy to
Identify data needed for submission -Can you handle internal and external data, structured and unstructured data, and future and historical data?
Translate your data to IDMP standards - Will you go through the cumbersome process of standardizing all your data manually? Or is there a way to automate it?
Face potential updates of the 2023 standards - Can you easily meet changes in standards after the launch of IDMP in 2023 or comply with standards for another organization at the same time?
Use IDMP to your advantage - Did you spot hidden gems in standardization? And how do you maximize results in the efforts needed to prepare for IDMP?
Demo video
How to use DISQOVER for IDMP submission
Learn how the DISQOVER platform can help you and your team in finding the information they need for IDMP submission.
