BERLIN + VIRTUAL

Join ArisGlobal at the GPRAS Summit

We’re looking forward to joining and presenting at this year’s GPRAS Summit, both in person and virtually 6-13 April 2022.

Our team will be available to meet with you to discuss your business challenges and you can catch our session – Regulatory Data: Empowering Teams to Drive Efficiencies across the Drug Development Lifecycle.

How We Can Help You

LifeSphere Regulatory delivers end-to-end regulatory information management in a unified cloud platform that accelerates approvals, reduces risk and streamlines collaboration across teams, and our IDMP solution has been named #1 in readiness.

Meet Our Team

Jim Hilferty

Jim Hilferty

Speaker

Robin Schilling

Robin Schilling

Speaker

Jessica Zito

Jessica Zito

Product Marketing

Kevin Smith

Kevin Smith

Sales

Event Details

If you’re attending in person, visit us at:

 

If you’re attending virtually, visit us at:

 

FACT SHEET
Speed. Quality. Collaboration.
Delivered in one simple unified platform

LifeSphere Regulatory delivers end-to-end regulatory information management in an all-new, fully unified cloud platform that accelerates speed to market, enhances data quality and streamlines collaboration across teams.

PRESS RELEASE
ArisGlobal’s LifeSphere IDMP Requirements, Readiness and Capabilities Acknowledged in Gens & Associates Reports
ArisGlobal currently has 19 of the 22 requirements available in their IDMP solution that were reviewed in the report, leading the other vendors evaluated. Gens’ industry report is a benchmark for IDMP vendors as they determine their cross-functional approach, improve automation as a core organizational goal and achieve IDMP/SPOR compliance.
WEBINAR

Regulatory Affairs Transformation Drivers for Small and Medium Life Sciences Companies

BLOG
Connected Data, Interoperability Enable Greater Compliance and Beyond
Most biopharmaceutical companies are still relying on legacy technology that siloes the pivotal arms of the organization. This is especially challenging for Regulatory teams, because these teams are tasked with both keeping their colleagues’ workflows compliant and carefully compiling data from across a drug candidate’s lifetime.
PARTNERS

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