Accelerating Global Submissions: How Industry Leaders Are Reducing Time to Market With the Accumulus Platform

A CUSTOMER FIRESIDE CHAT

April 22nd | 10 - 11 am EDT

A process that once took years, hundreds of interactions, and millions in cost can now be executed in months with a single shared submission—unlocking substantial operational and economic value at scale.

So, what do faster global approvals look like in practice and what results are customers seeing today?

Join us for a live fireside chat with leaders from Sanofi, Roche, and Amgen as they share the real-world impact they’re achieving with the Accumulus platform. In this candid conversation, you’ll hear firsthand how teams are accelerating global submissions, reducing time to market, and operating in a connected, real-time model of collaboration between industry and regulators—for the benefit of patients worldwide.

Hear directly from peers who have:

• Reduced global submission timelines by up to 90%
• Achieved up to 75% efficiency gains by eliminating manual coordination across markets
• Unlocked millions through faster, more efficient submissions

In this moderated discussion, panelists will share insights from real submissions and active use, including the challenges they set out to solve, lessons learned along the way, and the unprecedented impact of Accumulus Technologies’ Accelerated Collaborative Review Model.

 

Featured Speakers: 

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Melly Lin

Regional Policy Lead, Roche

 

Margaret Leahey

Senior Director,

Global CMC Biologics, Sanofi

J. Paul Kirwan

Senior Manager Global Regulatory Affairs CMC, Amgen

Complete your registration below!

Don’t miss this opportunity to hear directly from customers—sharing, in their own words, the results they’re seeing across submission timelines, team efficiency, and global regulatory coordination.

Thank you for your interest in Accumulus Technologies!

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