About this event
Webinar: Thursday 22nd June 2023 - 4pm CEST / 7am PDT / 9am CDT / 10am EDT
Learn more about the IDMP regulation, explore how structured content management can help streamline processes, and discover steps to prepare for the upcoming changes.
The Identification of Medicinal Products (IDMP) is a new regulatory standard affecting the packaging and regulatory content management processes for life sciences companies. ISO’s IDMP is a global regulatory framework for the standardization, identification, documentation, and exchange of pharmaceutical product information. The regulation is designed to improve patient safety, maximize pharmacovigilance, and ensure regulatory compliance across international borders.
Structured content management is a critical aspect of regulatory content management, and is becoming increasingly essential for life sciences companies to ensure compliance. In the context of IDMP, Structured Content management involves organizing, managing, and reusing medicinal product content in a format that facilitates easy access and sharing with regulatory authorities.
Attend the webinar to learn more about the IDMP regulation, explore how structured content management can help streamline processes, and discover steps to prepare for the upcoming changes.
Key takeaways will include:
- Understanding the IDMP regulation and its timeline
- The impact of IDMP on packaging and regulatory content management processes
- The importance of structured content management for IDMP compliance
- IDMP compliance best practices
Who should attend this webinar:
- Pharma Head of Packaging
- Pharma Head of Labeling
- Pharma Regulatory affairs professionals
- Pharma Labeling specialists
- Pharma Quality, pharmacovigilance professionals
- Pharma Product operations
- Risk management professionals for pharma
- Digital transformation, business systems Specialists
Hosted by
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Team member
Diana Fuentes Marketing Project CoordinatorDF T
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Guest speaker
Patrick Middag Director Regulatory & Compliance | Life Sciences & Healthcare @ Deloitte Risk AdvisoryG
Patrick has 25+ years of professional experience, educated as MSc. Applied Computer Sciences, complemented with an MBA from Vlerick Business School. His experiences include business technology solutions planning and implementation, enterprise architecture strategy, IT Business partnering, as well as serving in various project roles. Until recently and before joining Deloitte, Patrick was with Bristol Myers Squibb in Regulatory Affairs IT as an IT Business Partner and global lead for their IDMP program. Externally he represented Bristol Myers Squibb in various EFPIA expert working groups & forums and he collaborated with many pharma companies’ on their journeys towards IDMP compliance and implementations. He is passionate about the tremendous value that standardized, structured product information can bring to stakeholders, first and foremost to patients.
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Team member
Frederico MeloFM T
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Guest speaker
David Smith Technical Product Manager @ Esko I Brand SolutionsG
David L. Smith has +10 years of experience in the packaging and content space, helping to build a better artwork management solution. He enjoys gathering feedback from customers and understanding their use cases, in order to help provide better solutions and drive best practices.
Esko
Automate, Connect, AccelerateEsko is a global provider of integrated software solutions that accelerate the go-to-market process of packaged goods. We empower teams to support and manage the end to end packaging design and pre-production processes from Concept to Print.
