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The European Medicines Agency (EMA) is in the process of implementing the standards developed by the International Organization for Standardization for the identification of medicinal products (IDMP). Hear from top pharmaceutical company, Merck, on how they are keeping IDMP high on their agenda.
Pioneering their way on how to comply most efficiently, get a sneak peek into Merck's strategy to meet IDMP standards. As the former Data Governance Lead at Merck (current Sr. Director of the Data Value Office at BioNTech as of November 2022) and an advising member at the EU IDMP/SPOR Task Force, Dr. Jörg Werner focuses on both regulatory and compliance IDMP needs. Together with Tamara Stankovic, a Senior Data Solution Scientist at ONTOFORCE, they navigate through the dos and don'ts of a robust IDMP strategy.
While EMA is aiming to improve patient safety by standardization, their new regulation also introduces some data roadblocks.
Pioneering their way on how to comply most efficiently, Merck will share a sneak peek into their strategy to meet IDMP standards.
Linked data enables cross-domain data lineage for discovery and insight generation.
A technological deep dive in gathering data for an IDMP approved submission.