IDMP Readiness — How Pharma are Navigating the Complexities and Realizing Value, Upcoming Webinar Hosted by Xtalks


Pioneering their way on how to comply most efficiently, Merck will share a sneak peek into their strategy to meet IDMP standards.

How should one comply with the European Medicines Agency (EMA) Identification of Medicinal Products (IDMP)? Hear from a top pharmaceutical company, Merck, by 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.

Register for this webinar to learn:


  • How IDMP lines up with known data challenges in drug development. While EMA is aiming to improve patient safety by standardization, their new regulation also focuses on facilitating data roadblocks;
  • How to actively tackle these challenges with action-driven insights into how Merck uses data to add value to regulatory operations;
  • How IDMP opens new opportunities and linked data enables cross-domain data lineage for discovery and insight generation; and
  • How to bring an IDMP strategy to life and a technological deep dive in gathering data for an IDMP approved submission.

Join Dr. Jörg Werner, Data Governance Lead, Merck; and Tamara Stanković, Senior Data Solution Scientist, ONTOFORCE, for the live webinar on Tuesday, June 14, 2022, at 9am EDT (2pm BST/UK).

For more information, or to register for this event, visit IDMP Readiness — How Pharma are Navigating the Complexities and Realizing Value.

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