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The Reinvention of Life Science RegOps: is AI changing play?

At Breakthrough 2025, independent regulatory expert Preeya Beczek moderated the panel debate, Regulatory Operations: Driving Progress and Preparing for the Future.

From Planning to Launch: How to Implement a New Safety Database and Maximize ROI

At Breakthrough in Zurich, Felix Arellano, Global Head of Drug Safety at Roche, shared a candid and inspiring account of Roche’s multi-year journey to launch their next-generation safety system: Voyager.

AI is alive among us, whichever route we take: Boehringer Ingelheim’s takeaways from Breakthrough 2025

At Breakthrough 2025, Claudia Lehmann, Head of Global PSPV Operations at Boehringer Ingelheim, joined a user panel discussing the impact of NavaX, the powerful AI and machine learning engine which powers the platform.

Laying the foundations for a GenAI future: Roche’s journey

At Breakthrough 2025, Roche’s Jorge Carmona Toscano will join a panel discussion on emerging IT strategies to maximize the value of data and bed in greater GenAI use. 

Sharing data: lessons as Regulatory & Safety/PV teams get closer

At Breakthrough 2025, Hans van Leeuwen, Global Head of Regulatory Affairs Data & Systems at Astellas Pharma, will take part in a panel discussion on the pursuit of greater interoperability between Regulatory and Safety systems.

How to Make Your Case to Attend Breakthrough 2025: AI in Action

Are you eager to attend Breakthrough 2025 this March in Zurich but need to secure approval from your manager or team?

Extracting tangible value from AI in Regulatory Affairs, Compliance & More

In anticipation of a rousing Breakthrough 2025, Regulatory consultant and panel session moderator Preeya Beczek sets out her hopes for this year’s event.

Taking the pulse: how ready is the Regulatory function for AI-enabled reinvention?

Steve Gens previews some of the new research findings he’ll come armed with to a discussion panel on the future of Regulatory operations in an AI automation context. 

5 Reasons You Can’t Miss Breakthrough 2025

Breakthrough 2025 is set to be a pivotal event for safety, regulatory, and life sciences professionals.

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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