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.
On-demand Webinar
Learn from IDMP experts
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.
Checklist
Be well prepared
How confident are you at complying with the IDMP standards in the most efficient way?
Use the free Checklist for a solid and future-proof IDMP strategy and validate your organization's approach.
Factsheet
Digested for you
No time to read or watch the resources above?
We created an easy-to-understand summary of the most valuable insights and facts to improve your IDMP strategy.
Are you ready to improve your data to tackle your IDMP challenges?
