The Shift to the Cloud Historically, firms relied heavily on on-premises implementations for their enterprise solutions, including safety systems. Reliance…
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The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the processes for assessment and supervision of clinical trials…
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With up to 30-50% annual growth in adverse event cases, how are pharmacovigilance teams managing with today’s constrained budgets,…
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South Korean Contract Research Organization, LSK, spoke in a webinar with ArisGlobal to address the pressures of modernizing pharmacovigilance…
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ArisGlobal’s annual Breakthrough event is a one-of-a-kind event bringing together key leaders of the life sciences…
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Considering switching from a paper trial master file to an electronic one? There’s no better time than now. According to…
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The Future of Drug Safety Intelligence The future of safety intelligence is closer…
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As part of our commitment to providing the most robust out-of-the-box (OOTB) offering to our safety customers, we recently…
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Small and emerging biopharma like yours face a crucial question – should you outsource your drug safety system, or bring…
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