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Identification of Medical Products (IDMP) has been harmonizing data globally across the drug development lifecycle since 2003.

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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…

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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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ArisGlobal’s LifeSphere Regulatory Platform Brings Game-Changing  Efficiency to Life Sciences

If you are on the front lines of regulatory information management within the life sciences industry, you know how important…

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ArisGlobal Hosts Webinar Focusing on Regulatory Affairs Transformation Drivers for SMP Organizations

On May 14, 2020, ArisGlobal hosted a webinar titled Regulatory Affairs Transformation Drivers for Small and Medium Life Sciences Companies,…

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ArisGlobal to Present at the Global Regulatory Affairs Summit Digital Week

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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Webinar: The Future of Safety Signal Analytics is Now With LifeSphere Clarity   Learn more