
Identification of Medical Products (IDMP) has been harmonizing data globally across the drug development lifecycle since 2003. At its…
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Managing the submission of medicinal products, medical devices, and biologics to regulatory agencies is growing more complicated all the…
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When selecting an IDMP solution, remember decisions made today will impact the organization for years to come After a decade…
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Regulatory teams serve as the common thread of pharmaceutical research and development, connecting each domain on a drug’s journey to approval. Theirs…
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As the pharmaceutical industry adapts to a new world with a new set of challenges, it is critical to keep…
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BREXIT, the withdrawal of the United Kingdom (UK) from the European Union (EU) and the European Atomic Energy Community…
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Christina Johnston, Associate Director of Product Management for Regulatory at ArisGlobal, recently presented “AI Enhanced RIMS: What…
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If you are on the front lines of regulatory information management within the life sciences industry, you know how important…
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On May 14, 2020, ArisGlobal hosted a webinar titled Regulatory Affairs Transformation Drivers for Small and Medium Life Sciences Companies,…
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Christina Johnson, Associate Director Product Management Regulatory at ArisGlobal will be presenting at the Global Pharmaceutical Regulatory Affairs Summit Digital Week, on June 25th, 2020.
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