agEncoder™ : Request a Demo
agEncoder is a central coding solution that seamlessly integrates with ARISg, other safety case handling systems including Oracle Argus™, and other third-party tools such as clinical data...
View ArticleArisGlobal Launches TotalSafety 7.3
REGULATORY COMPLIANCE, INCREASED PRODUCTIVITY, QUALITY MANAGEMENT, AND LOWER TOTAL COST OF OWNERSHIP HIGHLIGHT PLATFORM UPGRADES Chicago, Illinois, October 4, 2016 — ArisGlobal announces the launch of...
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Becoming an Agile CRO with the ArisGlobal Pay-As-You-Grow Partner Program
By Phillip Strickland, Strategic Account Manager, Clinical Solutions In an article by Outsourcing Pharma earlier this year, it was reported that the global CRO market is expected to top $45 billion by...
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So You Have to Move off dsNavigator: How-to Advice on Switching Your Coding Tool
By Richard Jenkins With about a quarter of the life sciences market believed to be using Cerner’s dsNavigator coding tool, the decision to pull the solution from the market raises understandable...
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Recent Poll Confirms Top Challenges of Contract Research Organizations – and...
As cited in a recent blog, the Contract Research Organization (CRO) market is rapidly expanding. The flip side of this increased demand is that many CRO’s large and small are struggling to support what...
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You Know Where The Regulatory Submissions Gaps Are – Do You Know How To Fix...
Deploying a regulatory submissions management system is a critical challenge for many pharmaceutical companies as they wrestle with the vast amount of information exchanged within their own...
View ArticleA Holistic Approach to Drug Safety Reporting and Analytics
In an increasingly global environment, drug safety departments have been making significant investments in implementing common processes and systems to support operations in all regions. This may...
View ArticleAchieving Holistic View of Drug Safety Operations Metrics across the Enterprise
Achieving a holistic view of drug safety operations can be challenging given that the underlying data required to do so typically resides in multiple systems across the organization.Using agHub, life...
View ArticleLeveraging Multi-Tenancy for Cost Efficiencies
ARISg, the world’s leading pharmacovigilance and clinical safety system, has a rich set of features that help life sciences organizations comply with drug safety regulations across the globe. The...
View ArticleARISg and ARISj: Extending a Worldwide Pharmacovigilance Program into the...
An integrated safety and pharmacovigilance system with worldwide business processes helps companies realize significant productivity benefits. This position paper summarizes Aris Global’s Total Safety...
View ArticleAffiliate Safety Tracking
Aris Global has made great strides in delivering on the vision for achieving end-to-end paperless safety. This paper discusses the challenges that headquarters have in capturing all inbound safety...
View ArticleThe IRT Landscape: Regulations, Challenges and Solutions
Nearly all companies worthy of mention have received a letter containing one or several of these notifications: “You do not consistently report Adverse Drug Experiences (ADEs) within 15 days of initial...
View ArticleContinuous improvement of Pharmacovigilance systems as a driver for upgrade...
Over the years, life sciences organizations have made very few changes to their pharmacovigilance systems resulting in long upgrade cycles. This leads to difficulty in keeping up with regulations and...
View ArticleE2B (R3) and IDMP : Are you ready Webinars 2015
Adoption of the E2B (R3) electronic submission format for individual case safety reports (ICSRs) will require a significant effort from drug safety departments. E2B (R3) introduces a number of new...
View ArticleE2B(R3) compliance with Total Safety Webinars 2015
E2B (R3) compliance has multiple implications and triggers significant challenges for life sciences organizations at multiple levels: functional, technical and business. With EMA setting a timeline of...
View ArticleImplementation and Impact of new regulations on E2B (R3), eVAERS, eMDR for...
In 2013, the new E2B (R3) reporting guidance for transmission of Individual Case Safety Reports based on Health Level-7 (HL7) messaging protocol to outdated the existing E2B (R2) protocol. A clear...
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Survey Reveals Many Regulatory Submissions Management Systems Are Not...
Recent webinar, polls reveal challenges and future plans in regulatory submission processesDeploying an efficient regulatory submissions management system is a challenge for many pharmaceutical...
View ArticleRecent webinar, polls reveal challenges and future plans in regulatory...
Deploying an efficient regulatory submissions management system poses various challenges, including juggling vast amounts of information from disparate sources.Please fill in the below information to...
View ArticleWebinar-Regulatory Submissions Management Systems
The post Webinar-Regulatory Submissions Management Systems appeared first on ArisGlobal.
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Learn How Drug Safety Teams Can Overcome Resource Challenges
Pharmacovigilance and drug safety departments in life sciences companies must do more with less yet meet or exceed the same levels of quality and compliance. As case volumes and complexities increase,...
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