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...
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...
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...
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...
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...
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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