IDMP Readiness: how Pharma are Navigating the Complexities and Realizing Value

On demand Webinar

  • Price: Free

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.

What you will learn

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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.

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How Merck actively tackles this challenge and adds value

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

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How IDMP opens up new opportunities

Linked data enables cross-domain data lineage for discovery and insight generation.

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How to bring your IDMP strategy to life

A technological deep dive in gathering data for an IDMP approved submission.

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Speakers

Dr. Jörg Werner Data Governance Lead
MERCK
By aligning the data, there is a source of truth, and one can easily find what is connected.
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Tamara Stankovic Senior Data Solution Specialist
ONTOFORCE
Let's navigate through the dos and don'ts of a robust IDMP strategy with a live demo
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