How should one comply with the European Medicines Agency (EMA) Identification of Medicinal Products (IDMP)? Hear from a top pharmaceutical company, Merck, how they are keeping it high on their agenda.
Pioneering their way on how to comply most efficiently, Merck will share a sneak peek into their strategy to meet IDMP standards. As the data governance lead at Merck and an advising member at EU IDMP/SPOR Task Force, Dr. Jörg Werner focuses on both regulatory and compliance IDMP needs.
Together with Tamara Stanković, a Senior Data Solution Scientist at ONTOFORCE, they will navigate through the do’s and don’ts of a robust IDMP strategy.
While EMA is aiming to improve patient safety by standardization, their new regulation also focuses on facilitating 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.
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