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FiercePharma brings you an online event that will explore how companies can improve their electronic submission processes and protocols for RIM, and global regulatory submissions. With the goal of establishing a cohesive, compliant, and timely submission process in mind, our expert speaking faculty will discuss how to efficiently work with cross-functional stakeholders and optimize your team’s activities through the use of innovative technologies and processes.

Join us for the Virtual eRegulatory Operations Summit as we examine how to streamline your organization’s regulatory operations – in a new digital environment!

Event Highlights
  • Streamline your team’s regulatory processes by building a strong operational foundation
  • Identify changes in submission-related regulations impacting RIM business processes
  • Build inspection readiness into Your eRegulatory operations
  • Optimize regulatory information management from application to registration
  • Foster a digital document ecosystem in clinical trials
  • Explore the use of innovative tools and technology to increase the efficiency of your team

Featured Speakers:

Susan Hensley

Senior Director, Regulatory Operations, Regulatory Affairs Vaccines
TAKEDA PHARMACEUTICALS

Rick Arlow

Founder and CEO
COMPLION

Richard Fredericks

Director, Regulatory Systems and Information Management
GSK

Jessica Nardi

Senior Associate, Regulatory Systems & Information Management
GSK

Anne Marra

Head, Regulatory Operations
RA PHARMACEUTICALS, NOW A PART OF UCB

Craig Gassman

Director, Regulatory Operations and Quality Information Systems
VERICEL CORPORATION
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Francis Quinn

Director, US Publishing Hub Lead
PFIZER
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Carrie Mazzrillo

Associate Director, Regulatory Submission Management
VERTEX PHARMACEUTICALS

Jillian Carinci, MS

Associate Director, Regulatory Sciences
BIOGEN
Date: May 18, 2020
Start Time: 10:00AM ET