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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 ...

Transforming Life Sciences Agility on Both Sides of the Regulatory/Safety Sphere: A Year of Health Authority Successes

Learn how exciting new technological innovations are set to impact how regulatory information management teams work in 2024 and beyond.

5 New Innovations Set to Transform Regulatory Information Management

Learn how exciting new technological innovations are set to impact how regulatory information management teams work in 2024 and beyond.

Evolving Pharmacovigilance Beyond a Cost Center

Safety is evolving rapidly. There is a major, emerging opportunity ...

Regulatory Revolution: Unlocking the Era of Connected Insights

Nothing evolves within a vacuum. While today we can transmit ...

The Future of Pharmacovigilance Analytics and Insight

What will the next generation of reporting and analytics in ...

CTMS Solutions: Finding the Right Clinical Trial Management System

Managing a clinical trial is no small feat. Documents must ...

Unlocking the Next Generation of Reporting and Analytics for Drug Safety Intelligence

The Future of Drug Safety Intelligence The future of safety ...

12Next

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 220 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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