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The Future of Drug Safety Intelligence The future of safety intelligence is closer…

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ArisGlobal Announces the…

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Every person who wants to participate in clinical research should have the opportunity to do so…

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hands typing on

There’s no doubt that the pharmaceutical industry is well into its ‘age of automation’. A…

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looking at slide under microscope

Managing your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t…

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doctor discussing test results

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

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The coronavirus pandemic ushered in a new era of public scrutiny for the pharmaceutical industry. The general population was…

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Learn why Breakthrough is more than just an event but a summit for thought leaders in health and life sciences to discuss today and the future.

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The Digital Mindset in Drug Safety and Moving the Needle for your Organization

Digital Impact on the Drug Safety Space Digital transformation, automation, and analytics were top of mind when ArisGlobal recently…

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5 Key Takeaways From the 2021 DIA Medical Affairs and Scientific Communications Forum

The DIA Medical Affairs and Scientific Communications (MASC) Forum is created for medical affairs professionals by the best…

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ArisGlobal Acquires Leading Regulatory Data Governance Solution, SPORIFY
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