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Think Global, Watch Local: The DIA 2020 Annual Meeting Is Now Virtual, and ArisGlobal Is All In

The DIA 2020 Annual Meeting Is Now Virtual. ArisGlobal will be front and center with presentations covering both Safety and Clinical perspectives in Life Sciences process management.

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The Clinical Domain is Evolving. Make Sure your CTMS is Evolving with It.

The Evolving Role of CTMS in Risk Management takes a broad look at the challenges facing clinical trial management, how the clinical domain is changing, and how the industry can better respond.

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ArisGlobal’s LifeSphere CTMS10 Brings Complete Control and Full Visibility to Clinical Trials

A versatile Clinical Trial Management Solution, LifeSphere® CTMS10 contains great functionality and five key benefits, addressing a variety of challenges in the clinical product lifecycle.

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ArisGlobal’s LifeSphere MultiVigilance 10 Helps SMBs Manage and Master Pharmacovigilance

Managing and Mastering Pharmacovigilance covers how LifeSphere Multivigilance 10 benefits small to medium-sized businesses by utilizing industry-standard practices and proper management processes.

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ArisGlobal’s LifeSphere Mobile Has Evolved into LifeSphere Reporter. Here is What That Means for You.

A key offering in ArisGlobal’s LifeSphere platform, LifeSphere Reporter empowers field reps, provides fields teams and approved users with secure access, and easily integrates with LSMV10 and other systems.

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Presenting the All New Automation/Pharmacovigilance Knowledge Hub

ArisGlobal has created an Automation in Pharmacovigilance Knowledge Hub to help explain, in easily digestible terms, everything you need to know about automation in PV.

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ArisGlobal Hosts Optimizing Adverse Event Reconciliation in Medical Affairs Webinar

Many life sciences companies are still utilizing a manual process for their medical affairs needs. ArisGlobal’s LifeSphere ® Medical Affairs platform can help automate this process. Learn more about Medical Affairs and automated processes with our webinar, Optimizing Adverse Event Reconciliation in Medical Affairs.

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ArisGlobal Insights – Interview with Sandeep Mahagaonkar

This is the fourth in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety business units at ArisGlobal. Director of Product Management – Medical Affairs and Quality, Sandeep Mahagaonkar, spoke about what attracted him to ArisGlobal, the state of Medical Affairs, and the vision for 2020 and beyond.

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ArisGlobal Insights – Interview with Sondra Pepe

This is the first in a four-part blog series that examines the Clinical, Medical Affairs, Regulatory, and Safety product domains at ArisGlobal. Senior Director of Clinical Product Management, Sondra Pepe, describes what attracted her to ArisGlobal and articulated the vision for Clinical product strategy.

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Automation in Pharmacovigilance: A Real-World Implementation Story

In the last of our three-part blog series, we share the poll results to the question "What concerns do you have when it comes to automating PV process?" and analyze the responses. Read the blog to see how your responses might compare.

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