Top-five Global Life Sciences Company selects ArisGlobal enterprise-Level...
ArisGlobal’s LifeSphere® Safety Platform Provides Latest Advancements in AI and Cognitive Computing across All Organizational Business Units Miami, Florida – November 14, 2017 – ArisGlobal today...
View ArticleArisGlobal Is 1st Pharmacovigilance Solutions Provider to Successfully...
LifeSphere® Safety MultiVigilance gives customers a single, one-stop solution for providing full compliance with meeting EMA E2B R3 and avoids ‘work-around’ approach used by other pharmacovigilance...
View ArticleProductivity, Compliance and Quality: The Holy Grail in Pharmacovigilance
The pharmacovigilance landscape is evolving substantially with the changing regulatory environment and compliance requirements. With the increase in the number of drugs being approved by major...
View ArticleTCTM: Realizing Overall Business Improvements and Efficiencies with...
THE CLIENT NEED A full-service contract research organization headquartered in Dallas, Texas, Total Clinical Trial Management (TCTM), was eager to enhance its delivery model and quickly respond to its...
View ArticleIs Regulatory Affairs Ready for Automation?
The presentation explores productivity gains from automation in other settings to identify applicability for Regulatory professionals. Looking at Regulatory Information Systems in the context of E-2-E...
View ArticleArisGlobal appoints Sankesh Abbhi as President & CEO
Changing leadership will rapidly advance company’s focus on LifeSphere® cognitive computing platform Miami, Florida, 13 December 2017 –ArisGlobal, a leading provider of integrated, cloud-based...
View ArticleAutomation in Pharmacovigilance Data Processing – Do You Trust AI?
On November 28, 2017, ArisGlobal held a webinar with DIA, “How Automation Can Deliver the Holy Grail in Safety: Achieve Productivity, Compliance and Quality”. In this webinar, we posed a few...
View ArticleGetting Connected: The Benefits of a Unified Clinical Platform
Life Science Companies Make the Leap to Unified Platforms. In recent years, life science companies have struggled with clinical information technology chaos. Dysfunctional collections of clinical...
View ArticleIs Regulatory Affairs Ready for Automation? Part 1: What Is Your Greatest...
On December 6th, 2017, ArisGlobal held a webcast in partnership with DIA titled “Is Regulatory Affairs Ready for Automation?” In this webinar, our presenter, David Scanlon, Senior Director of...
View ArticleAchieving eTMF Success and Inspection Readiness” Matthias Poensgen, Clinical...
MIAMI, FLORIDA. January 11, 2018, 2017 — ArisGlobal, a leading provider of integrated, cloud-based software solutions for life sciences, announced that Mathias Poensgen, Clinical Subject Matter...
View ArticleNational Pharmacovigilance Systems Part 1: Pharmacovigilence with an ‘e’
The “4pt-classification” of the state of evolution of national pharmacovigilance systems This is the first in a three-part blog series on National Pharmacovigilance systems and the role of ‘e-...
View ArticleCognitive Computing in Pharmacovigilance: Revamping Drug Safety Using an...
Today’s pharmacovigilance department faces some of the most vexing issues facing life sciences companies. Among the major functions of a pharmacovigilance department, case management is considered to...
View Article“How Automation Can Deliver the Holy Grail in Safety”
Vivek Ahuja to present ArisGlobal Lunch-and-Learn session at DIA Pharmacovigilance and Risk Management Conference Miami, Florida, 15th January, 2018 – ArisGlobal, a leading provider of integrated,...
View ArticleIs Regulatory Affairs Ready for Automation? Part 2: Are you Ready for a ‘New’...
On December 6th, 2017, ArisGlobal held a webcast with DIA, “Is Regulatory Affairs Ready for Automation?” In this webinar, our presenter, David Scanlon, Senior Director of Regulatory Strategy, posed...
View ArticleRegulatory 2025: Developing an effective 10-year strategy for...
Preparing to meet regulatory and commercial demands of the future requires a progressive, future-proof approach. As the regulatory department prepares for 2020 and the rest of the decade it must...
View ArticleNational Pharmacovigilance Systems Part 2: Modern Technologies in...
This is the second in a three-part blog series on National Pharmacovigilance systems and the role of technology in bridging the gaps in pharmacovigilance of regulatory authorities around the world....
View ArticleIs Regulatory Affairs Ready for Automation? Part 3: Rating Your...
On December 6th, 2017, ArisGlobal held a webinar with DIA, “Is Regulatory Affairs Ready for Automation?” In this webinar, our presenter, David Scanlon, Senior Director of Regulatory Strategy, posed...
View ArticleNational Pharmacovigilance Systems Part 3: Advanced Pharmacovigilance...
This is the third in a three-part blog series on National Pharmacovigilance systems and the role of technology in bridging the gaps in pharmacovigilance of regulatory authorities across the world....
View ArticleUnified LifeSphere® CTMS and LifeSphere® EDC Help SIRO Clinpharm Improve...
Leading Indian CRO enters partnership with ArisGlobal to enhance its delivery capability in operations and biometrics Miami, Florida, January 30, 2018 — ArisGlobal, a leading provider of integrated...
View ArticleRe-Think Your Integrated CTMS: Why Moving to Unified Platform is the Only...
Most sponsors and clinical research organisations manage clinical trials using an average of three to five independent core systems. Creating duplicate data and processes in multiple systems impacts...
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