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Unlocking the Strategic Value of Pharmacovigilance

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GenAI’s large language models will transform safety & regulatory processes

Up to now, AI technology has had to be painstakingly ‘trained’ in what to look for.

Embracing the Cloud: A Transformative Journey in Regulatory Operations

In the ever-evolving world of pharmaceuticals, a leading company has embarked on a transformative journey by moving its regulatory operations to the cloud.

Transforming Medical Affairs Engagement with Generative AI

In today's rapidly evolving landscape of medical affairs, stakeholder engagement ...

Revolutionizing Data: The Power of Advanced Intake

In the ever-evolving landscape of data management, the life sciences ...

How LifeSphere Medical Information Transformed Medical Information Management at a Leading European Pharma Company

In the highly competitive pharmaceutical industry, efficiently managing medical information ...

Visionaries Take Center Stage: Honoring Trailblazers at the 2024 Breakthrough Awards

ArisGlobal celebrates customers that are reaching new heights via LifeSphere ...

Why cloud is the only modern option for efficient, high-volume Safety data processing

Sam Wallis, Head of ICSR Case Processing within the Worldwide Patient Safety Operations at Bristol Myers Squibb, will join a Breakthrough 2024 panel discussion on the reality of transitioning Safety/Regulatory systems to the cloud. Here, he provides a glimpse into BMS’s own journey, which he’ll share candidly during the Day 1 debate.

Regulatory process transformation – including closer collaboration with Safety/PV – starts with cloud-based RIM

At Breakthrough 2024 this month, Hans van Leeuwen, Head of RA Data and Systems Excellence at Astellas Pharma, will deliver a keynote on the company’s journey to the cloud for regulatory information management.

Top Reasons to Attend Breakthrough2024

ArisGlobal’s annual Breakthrough is a one-of-a-kind event bringing together industry ...

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ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 500 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.

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