There’s no doubt that the pharmaceutical industry is well into its ‘age of automation’. A…
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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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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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Digital Impact on the Drug Safety Space Digital transformation, automation, and analytics were top of mind when ArisGlobal recently…
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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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It’s hard to think about COVID-19 and vaccine production, without reflecting on the speed, safety, and risks involved…
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As the pharmaceutical industry adapts to a new world with a new set of challenges, it is critical to keep…
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