We Bring the Future to Life
ArisGlobal is a leading provider of cloud-based software solutions for Pharmacovigilance & Drug Safety, Clinical Development, Regulatory, and Medical Affairs
ArisGlobal Life Sciences Technology Summit 2019
Oct 1 – 3, 2019 | The Miami Beach EDITION | Miami, FL. USA
The LifeSphere® Platform
Powered by Nava
LifeSphere is an end-to-end life sciences platform, using ArisGlobal’s proprietary Nava® cognitive computing engine to automate all core functions of the drug development process. Offering simple integration with our next-generation LifeSphere EasyDocs document management solution across the product lifecycle, the LifeSphere platform helps life sciences companies reduce time to market, increase compliance and lower drug development costs.
LifeSphere®
Clinical Development
LifeSphere®
Regulatory
LifeSphere®
Safety
LifeSphere®
Medical Affairs
LifeSphere®
Quality
LifeSphere®
EasyDocs
seamlessly woven into the entire LifeSphere ecosystem.
The LifeSphere® Platform
Powered by Nava
LifeSphere is an end-to-end, cloud-based software platform, using ArisGlobal’s proprietary Nava® cognitive computing engine to automate all core functions of the drug development process. Offering simple integration with our next-generation LifeSphere EasyDocs document management solution across the product lifecycle, the LifeSphere platform helps life sciences companies reduce time to market, increase compliance and lower drug development costs.
LifeSphere®
Clinical Development
LifeSphere®
Regulatory
LifeSphere®
Safety
LifeSphere®
Medical Affairs
LifeSphere®
Quality
LifeSphere®
EasyDocs
Delivering Real Results to a Global Client Base
Delivering Real Results to a Global Client Base
80%
of the top 50 pharma companies are our clients
30%
immediate cost saving potential via our advance automation capabilities
80%
potential efficiency gains driven by our Nava cognitive computing engine.
100%
compliance with all present and upcoming regulatory standards.
Working with Some of the Industry’s Best
Working with Some of the Industry’s Best
What Our
Customers are Saying
“Our decision to upgrade to LifeSphere Safety MultiVigilance was based on better integration, improved case management, reduced costs, and the ability to reach even higher compliance requirements of our customers and regulators.”
Ravi Menon
Chairman of the Board,
APCER Life Sciences
“Advanced technology, such as artificial intelligence and machine learning, are key LSMV capabilities that help us automate repetitive, manual tasks, thus improving efficiency and compliance. By switching to LifeSphere Safety MultiVigilance, our efforts to comply with regulations will be much more efficient.”
Fosun Pharma
“We have seen how the LifeSphere platform’s advanced robotic automation and cognitive features will allow us to automate many of our key PV steps in the area of case processing, which are currently resource intensive”
Claudia Lehmann
Head of PV Operations,
Boehringer Ingelheim
News
Press Release:
LifeSphere Publishing
A Comprehensive Solution for Compiling, Publishing and Validating Regulatory Submissions
Press Release:
LifeSphere EasyDocs
A Unified Platform to Streamline Enterprise
Document Management Across the Product Lifecycle
World Drug Safety Congress Europe, 10 – 11 Sept
How to Fully Leverage Automation in PV – Real Case Study.
Presented by:
Aman Wasan, VP for Global Pharmacovigilance, ArisGlobal
10 Sept, at 2:10pm CET | Amsterdam
Press Release:
LifeSphere Publishing
A Comprehensive Solution for Compiling, Publishing and Validating Regulatory Submissions
Press Release:
LifeSphere EasyDocs
A Unified Platform to Streamline Enterprise
Document Management Across the Product Lifecycle
Thought Leadership
Regulatory Structured Authoring: Next Steps in Achieving Greater Efficiencies and Consistency
Blog
Regulatory Structured Authoring: Next Steps in Achieving Greater Efficiencies and Consistency
Moving to a structured content authoring approach presents the challenge of ensuring that data and documents are in sync. So where do life sciences organizations stand today in this transformation phase? Wim Cypers, Senior VP, Regulatory, shares his insights from our recent webinar.
Blog
Moving to Self-Service: A Key Component of an Effective Automated Content Management Strategy for Medical Information Managers
