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AI, Cloud and Other Advanced Technology: Organizational Readiness Is at the Center of This Transformation Journey

Pharmaceutical companies, service providers, and solution providers should focus on as technology advancements continue to transform drug safety for the future. Read the blog

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“Are You Ready for the New Era in PV?” to be Presented by ArisGlobal’s VP of Global PV at World Drug Safety Congress

ArisGlobal, LLC, a leading provider of life sciences software will present a session titled “Are You Ready for the New Era in PV?” at the upcoming World Drug Safety Congress Americas 2019

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AI, Cloud and Other Advanced Technology: Are You Ready for the New Era of Drug Safety?

LifeSphere Safety MultiVigilance (LSSMV) database system has auto-translation capabilities that can translate safety narratives from English to Chinese and vice versa using advanced machine-learning technology.

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“Towards Regulatory 2025” to Be Presented by ArisGlobal Regulatory Expert at eRegulatory Summit 2019

ArisGlobal Safety Experts to Present “Supporting Life Science Industry to Meet the New Regulation Challenges” at 9th Asia Pharma R&D Leaders – Pharma & Healthcare

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ArisGlobal Launches LifeSphere Publishing as Key Component of LifeSphere Regulatory Cloud Platform

LifeSphere Publishing is an advanced, ,multi-tenant cloud submissions management system that enables life science organizations to easily compile, publish, and validate regulatory submissions with full support for all major global eCTD requirements

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ArisGlobal Launches Enterprise-Level Document Management Platform

LifeSphere EasyDocs is a highly configurable, advanced cloud platform architected to streamline and unify enterprise document management and provide continuity of cross-functional workflows across the full drug development process

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The ‘Learning’ Pharmacovigilance System : From Concept to Reality

While experiential learning has been true for humans, it is now increasingly becoming a reality for machines. Machines and Systems are becoming “intelligent” and “smart,” capable of learning and

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Creating a Unified Clinical and Regulatory Data Management Strategy

Examining the challenges involved, benefits to be gained and requirements of unified regulatory and clinical business processes, as well as recommendations for taking the next steps forward.

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The Future of Regulatory Affairs

ArisGlobal Safety Experts to Present “Supporting Life Science Industry to Meet the New Regulation Challenges” at 9th Asia Pharma R&D Leaders – Pharma & Healthcare

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Download ArisGlobal’s 2024 Industry Report   Learn More

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