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  • COST: FREE
  • Duration: 29 min

IDMP readiness: how pharma are navigating the complexities and realizing value

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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, Merck shares a sneak peek into their strategy to meet IDMP standards. As the data governance lead at Merck and an advising member at the EU IDMP/SPOR Task Force, Dr. Jorg 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.

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 introduces some 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.

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.
Dr. Jörg Werner DATA GOVERNANCE LEAD MERCK
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
TAMARA STANKOVIC Customer Data Scientist DISQOVER Platform ONTOFORCE
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