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Join Us At:

DIA Regulatory Submissions,
Information and Document Management

February 10-12, 2020 | North Bethesda, MD, US | Booth #312

Join Us At:

DIA Pharmacovigilance and Risk Management Strategies Conference

Jan 27 – 29, 2020 | Washington DC, US | Booth #24

Join Us At:

Arab Health 2020

Jan 27 – 30, 2020 | Dubai, UAE | Booth #PZ.F31

Press Release

Industry’s Largest Drug Safety System Implementation

ArisGlobal’s LifeSphere® MultiVigilance Goes Live with Top 5 Pharma, Delivering a Next-Gen Safety System to 2,300+ End Users.

Press Release

FDA Selects ArisGlobal’s LifeSphere MultiVigilance as its Next-Generation Safety Platform

Announcing the launch of our newest offerings:

Announcing the launch of our newest offerings:

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

End-to-end platform seamlessly linking clinical operations and clinical data management via unified architecture; designed for easy integration with our LifeSphere Regulatory solutions.

Learn More

LifeSphere®

Regulatory

Comprehensive RIMS platform – including our new Publishing solution – providing a single source of truth across the entire regulatory organization and compliance with xEVMPD and IDMP standards.

Learn More

LifeSphere®

Safety

Next-generation platform for intelligent, machine-learning enhanced processing of adverse events and individual case safety reports; from automated intake to advanced signal detection and risk management.

Learn More

LifeSphere®

Medical Affairs

The only platform to support all medical information functions within a single integrated workspace, providing a unified solution for inquiry receipt, fulfillment, adverse events, product complaints, and reporting.

Learn More

LifeSphere®

Quality

Our newest offering, built from the ground up on LifeSphere’s cloud architecture and providing industry-leading capabilities across product complaints and quality management. Arriving 2020.

Learn More

LifeSphere®

EasyDocs

A highly configurable, enterprise-grade document management solution,
seamlessly woven into the entire LifeSphere ecosystem.

Learn More

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

End-to-end cloud platform that seamlessly links clinical operations and clinical data management via unified architecture; designed for easy integration with our LifeSphere Regulatory solutions.

Learn More

LifeSphere®

Regulatory

Comprehensive RIMS platform – including our new Publishing solution – providing a single source of truth across the entire regulatory organization and compliance with xEVMPD and IDMP standards.

Learn More

LifeSphere®

Safety

Next-generation platform for intelligent, machine-learning enhanced processing of adverse events and individual case safety reports; from automated intake to advanced signal detection and risk management.

Learn More

LifeSphere®

Medical Affairs

The only platform to support all medical information functions within a single integrated workspace, providing a unified solution for inquiry receipt, fulfillment, adverse events, product complaints, and reporting.

Learn More

LifeSphere®

Quality

Our newest offering, built from the ground up on LifeSphere’s cloud architecture and providing industry-leading capabilities across product complaints and quality management. Arriving Summer 2019.

Learn More

LifeSphere®

EasyDocs

A highly configurable, enterprise-grade document management solution, seamlessly woven into the entire LifeSphere ecosystem.

Learn More

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 savings potential via our advanced automation capabilities
80% potential efficiency gains driven by our Nava cognitive computing engine
100% compliance with all present and upcoming regulatory standards

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.

LifeSphere MultiVigilance 10

 

Intelligent and Automated Safety Platform for Individual Case Safety Report Processing

 

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

Join Us At:

DIA Pharmacovigilance and Risk Management Strategies Conference

Jan 27 – 29, 2020 | Washington DC, US | Booth #24

Learn More

Join Us At:

Arab Health 2020

Jan 27 – 30, 2020 | Dubai, UAE | Booth #PZ.F31

Learn More

Join Us At:

DIA Regulatory Submissions,
Information and Document Management

February 10-12, 2020 | North Bethesda, MD, US | Booth #312

Learn More

Join Us At:

DIA Pharmacovigilance and Risk Management Strategies Conference

Jan 27 – 29, 2020 | Washington DC, US | Booth #24

Learn More

Join Us At:

Arab Health 2020

Jan 27 – 30, 2020 | Dubai, UAE | Booth #PZ.F31

Learn More

Join Us At:

DIA Regulatory Submissions,
Information and Document Management

February 10-12, 2020 | North Bethesda, MD, US | Booth #312

Learn More

Thought Leadership

Infographic

Global ICH E2B (R3) Implementation

Infographic

Global ICH E2B (R3) Implementation

The primary purpose of ICH E2B (R3) is to achieve consensus in safety reporting and harmonization of data for global electronic exchange. In reality, there might be several regional differences. Discover how and when 11 global Regulatory Authorities plan to implement ICH E2B (R3) standards.

Blog

Automation in Pharmacovigilance: A Real-World Implementation Story

Learn More

Blog

Automation in Pharmacovigilance – Choose Your Own Adventure

Learn More

Blog

ArisGlobal Differentiates Automation Hype from Reality in Pharmacovigilance for the Life Sciences Industry

Learn More

UPCOMING EVENTS

Connect with ArisGlobal’s Life Sciences Experts at our 2020 Events

CONTACT US



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