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Christina Johnston, Associate Director of Product Management for Regulatory at ArisGlobal, recently presented “AI Enhanced RIMS: What…

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Best Practices for Digitally Transforming Pharmacovigilance Processes

On June 9th, 2020 ArisGlobal held a webinar titled “Pharmacovigilance and Digital Transformation: Stepping…

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Digitally Transforming Pharmacovigilance Processes Remains a Key Life Sciences Priority

On June 9, 2020 ArisGlobal held a webinar titled “Pharmacovigilance and Digital Transformation: Stepping into the Technology-Driven…

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ArisGlobal Presented “The Evolving Role of CTMS in Risk Management” at DIA 2020 Annual Meeting

On June 16th, 2020, ArisGlobal participated in the 2020 DIA Annual Meeting, where Sondra Pepe, Senior…

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As evident from our second polling question, ”How far along the road would you say you are for a ‘new’ technological revolution,” the journey to capitalize on the next industrial revolution is just beginning for most participants

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As evident from our second polling question, ”How far along the road would you say you are for a ‘new’ technological revolution,” the journey to capitalize on the next industrial revolution is just beginning for most participants

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Automation technologies are having a major impact on performance and productivity across industries. In regulatory, these technologies also have the potential to reshape many activities across regulatory, leading to significant productivity gains. While there’s a lot of talk about how automation technologies will create new roles with exciting opportunities, the most powerful impact will be on the data quality and the efficiency with which manual tasks will be accomplished.

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Mobility and Medical Affairs: Enabling Communication and Collaboration across the Stakeholder Spectrum – Part 1

“The most competitive pharma companies in the coming decade will be masters of data and digital technologies.” So begins the June 2017 industry brief, “Reinventing the Role of Medical Affairs,” by Bain & Company.

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From reporting challenges to data integration and data silos with clinical data management, to the continuing search for greater automation,…

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Connected to the Future: Making Drug Safety Databases Transparent, E2B R3 Compliant and Cost-Effective

As different regulatory authorities have different timelines for adoption of these standards, E2B(R2) E2B(R3) will have to coexist. But having to operate two solutions creates huge complexities, unless you find a solution compliant with both. ArisGlobal LifeSphere Safety MultiVigilance is the only drug safety database solution provider thus far to provide full compliance to E2B R2 and E2B R3 standards for both import and export.

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