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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
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Impacting People's Lives
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
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Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
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Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
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Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
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"At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.
VIEW ROLESWebinar
Is your organization IDMP ready?
July 29, 2021
Calendar
11:00am - 12:00pm
GMT-04:00
After delays and uncertainty, the countdown to IDMP is getting closer. The EMA will be the first health agency to mandate compliance with ISO IDMP, with the FDA not far behind. Pharma organizations face a rapidly shortening timeframe to prepare for full transition of regulatory data and systems to comply with this complex mandate.
Publication of the EU Implementation Guidelines v2 in February 2021 started the 2-year implementation window. EU IG V2.1 is due out in June 2021. And, in Q1 2022, the EMA expects pharma companies to be able to submit product data in IDMP format, and by Q1 2023, this will be mandatory.
IDMP (Identification of Medicinal Products) refers to a set of standards designed to standardize the structure and terminology used to describe marketed medicinal products. IDMP's primary goal is to enhance patient safety by improving the speed, accuracy, consistency, and sharing of adverse events and safety signal reporting globally.
Capturing the hundreds of data entities required per product, 70% of which lie in unconnected silos of unstructured text, demands time, resources, and investment.
However, manual curation is not the only option for extraction of the necessary data attributes. Linguamatics NLP text mining solution can save your organization significant time and reduce mistakes on its IDMP-compliance journey.
In this webinar, we will discuss the application of Linguamatics NLP for the extraction of key data elements from unstructured text, using Summary of Product Characteristic documents as an example.
Who should attend?
Directors and managers in regulatory affairs, operations, compliance; plus, information and knowledge management professionals responsible for master data management strategies, regulatory information management, IDMP implementation.
Speakers
Jane Reed
Director of Life Science Linguamatics, an IQVIA company
Yannis Haldoupis
Senior Application Scientist Linguamatics, an IQVIA company