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.
How should one comply with the European Medicines Agency (EMA) Identification of Medicinal Products (IDMP)?
Hear from Dr. Jörg Werner, Data Governance Lead at Merck, about how they are keeping it high on their agenda.
Additionally, Tamara Stanković, a Senior Data Solution Scientist at ONTOFORCE, will navigate through the dos and don’ts of a robust IDMP strategy.