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Lifting the Tedium of Medical Literature Monitoring with Automation

One of the key roles of pharmacovigilance departments is to understand the benefit-risk profile of a drug. But departments are often bogged down by manual tasks that can absorb time, which might be better spent on value-centric activities. Perhaps the most tedious pharmacovigilance activity is medical literature monitoring (MLM), and as we discussed in our last blog, manual, repetitive tasks are a primary cause of employee dissatisfaction.

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Survey Finds Slow But Steady Move toward a Unified Clinical Platform

During a recent webcast, ArisGlobal carried out an insightful survey, which found that visibility and reporting inefficiencies remain a headache.

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National Pharmacovigilance Systems & Role of Technology in Bridging the Disparities

Download this white paper to learn about. Pharmacovigilance with an ‘e’ – the “4pt-classification” of the state of evolution of national pharmacovigilance systems Modern technologies in pharmacovigilance system – the way forward for national PV systems Advanced pharmacovigilance technologies –the role ‘e- enablement’ technology plays in bridging the gaps in pharmacovigilance of regulatory authorities across the world

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ArisGlobal Announces LifeSphere® Publishing and LifeSphere® Analytics to Streamline Regulatory Submissions and Reporting

ArisGlobal, a leading provider of integrated cloud-based software solutions for life sciences, announces LifeSphere Publishing and LifeSphere Analytics, new solutions that will integrate with LifeSphere RIMS™ and LifeSphere IDMP™ to offer the most complete, unified platform for regulatory affairs. LifeSphere Publishing delivers streamlined publishing capabilities and content management, and LifeSphere Analytics ensures all reports and analyses will comply with regulatory requirements.

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Tags: adverse event Pharmacovigilance
Benefits & Challenges of Artificial Intelligence in Pharmacovigilance

Pharmacovigilance is at a crossroads. The best, most innovative way forward for PV departments may well be automation, as they address the challenges (or market pull factors) and opportunities (or technology push capabilities).

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Medical Information: Easy Integration of LifeSphere® MI with Your Chosen CRM Lets You Have Your Cake and Eat It Too

As a medical information software provider, it is necessary to recognize that there is some decent software out there in the life science’s space

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Re-Think Your Integrated CTMS: Why Moving to Unified Platform is the Only Path Forward

Most sponsors and clinical research organisations manage clinical trials using an average of three to five independent core systems. Creating…

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Tags: ArisGlobal Press Release lifesphere clinical
Unified LifeSphere® CTMS and LifeSphere® EDC Help SIRO Clinpharm Improve Clinical Trial Management Productivity and Efficiency

Leading Indian CRO enters partnership with ArisGlobal to enhance its delivery capability in operations and biometrics…

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National Pharmacovigilance Systems Part 3: Advanced Pharmacovigilance Technologies – A Solution for Deficiencies

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.

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Tags: ArisGlobal Blogs regulatory affairs regulatory information management

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 beginning for most participants

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Download ArisGlobal’s 2024 Industry Report   Learn More
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