Signal Detection & eRMR: New EudraVigilance System Is Almost Here – Are You...
For many companies, signal detection in drug safety pharmacovigilance ranks closely behind regulatory submissions and case management as a key activity because it helps to proactively monitor a...
View ArticleMobility and Medical Affairs: Enabling Communication and Collaboration –...
Our first blog on this topic addressed “The importance of mobility and medical affairs (MA) and its value to the organization is most definitely on the rise.” In this concluding blog we share specific...
View ArticleEMA SPOR Working group release the details to the SPOR Change Liaison Group
EMA SPOR Working group release the details to the SPOR Change Liaison Group for bringing Industry on-board the Organisational Management Service (OMS) and Referential Management Service (RMS), which...
View ArticleTaking a Best Practices Approach to Safety Signal Detection and Risk Management
Life sciences companies confront increasingly stringent requirements on safety signal detection and risk management. Regulatory authorities are taking steps to further safeguard patients by requiring...
View ArticleArisGlobal Regulatory Expert to Present at eRegulatory Summit on Industry...
CHICAGO, IL. APRIL 7, 2017–ArisGlobal, LLC, a global leader in providing cloud-based software solutions for the life sciences, has announced that Pratyusha Pallavi, Product Manager for Regulatory, will...
View ArticleTop-five Global Life Sciences Company selects ArisGlobal enterprise-Level...
ArisGlobal today announced that a top-five global life sciences company based in the U.S. selected ArisGlobal’s LifeSphere Safety cloud solution suite as its enterprise-level pharmacovigilance and drug...
View ArticleArisGlobal Is 1st Pharmacovigilance Solutions Provider to Successfully...
LifeSphere Safety MultiVigilance is the first pharmacovigilance solution (version 7.4.1.1-HF1) to have successfully completed E2B R3 testing with the XCOMP EudraVigilance system. Organizations using...
View ArticleProductivity, Compliance and Quality: The Holy Grail in Pharmacovigilance
This webinar details how organizations can counter these challenges and become more sophisticated in their drug-related adverse event reporting by adopting state-of-the-art cognitive computing...
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 software...
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 questions...
View ArticleGetting Connected: The Benefits of a Unified Clinical Platform
The constant and critical push to accelerate a product’s time to market continues to push clinical teams to seek solutions that deliver greater efficiencies. But after 20 years of... The post Getting...
View ArticleIs Regulatory Affairs Ready for Automation? Part 1: What Is Your Greatest...
Automation technologies are having a major impact on performance and productivity across industries. In regulatory, these technologies also have the potential to reshape many activities across...
View ArticleAchieving eTMF Success and Inspection Readiness” Matthias Poensgen, Clinical...
The post Achieving eTMF Success and Inspection Readiness” Matthias Poensgen, Clinical Expert at ArisGlobal Speaks at Trial Master File Summit appeared first on ArisGlobal.
View ArticleNational Pharmacovigilance Systems Part 1: Pharmacovigilence with an ‘e’
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 questions...
View ArticleCognitive Computing in Pharmacovigilance: Revamping Drug Safety Using an...
Cognitive computing has the potential to revamp the practice of pharmacovigilance, from a tedious, resource-intensive process to a dynamic and efficient practice. The post Cognitive Computing in...
View Article“How Automation Can Deliver the Holy Grail in Safety”
ArisGlobal, a leading provider of integrated, cloud-based software solutions for life sciences, announced that Vivek Ahuja, Vice President, Global Pharmacovigilance at ArisGlobal, will present a...
View ArticleIs Regulatory Affairs Ready for Automation? Part 2: Are you Ready for a ‘New’...
As evident from our second polling question, ”How far along the road would you say you are for a ‘new’ technological revolution,” the journey to capitalize on the next industrial revolution is just...
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 The post Regulatory 2025: Developing an...
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