This webinar presented an overview of the end-to-end testing results for the Global Pharmaceutical Product Identification (PhPID) Service operating model, which generates global PhPIDs for marketed medicinal products. The session detailed the model’s readiness for deployment, including its software functionality, interoperability, processes, and business rules.
Timestamps
00:56 – Global IDMP Implementation: Getting Closer to the Goal
12:20 – GIDWG Global IDMP Identifiers
47:37 – Global IDMP Implementation: Readiness
01:05:57 – Q&A Session
Speakers | Panelists:
Ron Fitzmartin, PhD, MBA
Sr. Advisor
Data Standards Branch
Office of Regulatory Operations
Center for Biologics Evaluation and Research
Ta-Jen Chen
Project Management Officer
Office of Strategic Programs
Center for Drug Evaluation and Research
Olof Lagerlund, PhD
Substance Expert
Uppsala Monitoring Centre
WHO Collaborating Centre for International Drug Monitoring
Learn more at: https://www.fda.gov/drugs/news-events-human-drugs/global-idmp-implementation-getting-closer-goal-10162024
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