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Home / Blogs / Regulatory - Blogs

Not Your Average RIMS: Managing Increasing Complexity in Regulatory Affairs

by Kiera Blessing | Apr 18, 2022 | Blogs, Regulatory - Blogs, Uncategorized

Managing the submission of medicinal products, medical devices, and biologics to regulatory agencies is growing more complicated all the time. To streamline the processes that go into creating and tracking these submissions, life science organizations are increasingly...

To Prepare for IDMP, Organizations Must Think Years Ahead – Not Months

by Kiera Blessing | Mar 7, 2022 | Blogs, Regulatory - Blogs, Uncategorized

When selecting an IDMP solution, remember decisions made today will impact the organization for years to come After a decade of preparation, the new Identification of Medicinal Products (IDMP) standard is poised to go into effect in a few short months.  The impending...

Connected Data, Interoperability Enable Greater Compliance and Beyond

by Kiera Blessing | Jan 17, 2022 | Blogs, Regulatory - Blogs, Uncategorized

Regulatory teams serve as the common thread of pharmaceutical research and development, connecting each domain on a drug’s journey to approval. Theirs is the only function that plays a role in every stage of bringing a drug to market, from initial research through...

Examining The Unified Future of Regulatory Platforms With Astellas

by Ethan Roberson | Apr 28, 2021 | Blogs, Regulatory - Blogs

As the pharmaceutical industry adapts to a new world with a new set of challenges, it is critical to keep global teams aligned. There’s more emphasis on speed, efficiency and collaboration than ever and the need for it to be delivered in an end-to-end unified platform...

How to Manage BREXIT Changes with LifeSphere RIMS

by Ethan Roberson | Apr 13, 2021 | Blogs, Regulatory - Blogs

BREXIT, the withdrawal of the United Kingdom (UK) from the European Union (EU) and the European Atomic Energy Community (EAEC or Euratom), has changed the way business is done in a wide variety of industries. Since the pharmaceutical industry is the third largest...

AI Enhanced RIMS: What the Future Holds for Regulatory

by Alberto Cantor | Aug 14, 2020 | Blogs, Regulatory - Blogs

Christina Johnston, Associate Director of Product Management for Regulatory at ArisGlobal, recently presented “AI Enhanced RIMS: What the Future Holds” as part of the Global Pharmaceutical Regulatory Affairs Summit Digital Week. During the presentation, Christina...
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    About ArisGlobal®

    ArisGlobal is transforming the way today’s most successful Life Sciences companies develop breakthroughs and bring new products to market. Our end-to-end drug development technology platform, LifeSphere®, integrates our proprietary cognitive computing engine to automate all core functions of the drug development lifecycle. Designed with deep expertise and a long-term perspective that spans more than 30 years, LifeSphere® is a unified platform that boosts efficiency, ensures compliance, delivers actionable insights, and lowers total cost of ownership through multi-tenant SaaS architecture.

    Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China. For more updates, follow ArisGlobal on LinkedIn and Twitter.

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