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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.

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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 Transformation is Accelerating Digital transformation, automation and analytics were top of mind when ArisGlobal recently hosted a thought…

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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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Contract Research Organizations (CROs) have been enthusiastic early adopters of the LifeSphere electronic Trial Master File…

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Get the Guide: When and How to Choose Your First Safety System   View Now

LifeSphere Clarity: The future of safety signal analytics has arrived.

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