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CTMS Solutions: Finding the Right Clinical Trial Management System

Managing a clinical trial is no small feat. Documents must ...

Benefits of a True SaaS Safety System

The Shift to the Cloud Historically, firms relied heavily on ...

3 Changes (and Benefits) of the EU Clinical Trials Regulation

The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the ...

Best Practices in Safety Signal Analytics — Managing Today and Preparing for Tomorrow

With up to 30-50% annual growth in adverse event cases, how ...

How Leading South Korean Biopharma LSK is Modernizing Pharmacovigilance Operations with ArisGlobal

South Korean Contract Research Organization, LSK, spoke in a webinar ...

5 Reasons to Attend Breakthrough This Year

ArisGlobal’s annual Breakthrough event is a one-of-a-kind event bringing together ...

7 Things to Consider When Moving to an eTMF (Electronic Trial Master File) System

Considering switching from a paper trial master file to an ...

Unlocking the Next Generation of Reporting and Analytics for Drug Safety Intelligence

The Future of Drug Safety Intelligence The future of safety ...

Turnkey Configuration and Next Level Standardization: ArisGlobal Works with Industry Leaders to Optimize Out-of-the-Box Safety Workflow

As part of our commitment to providing the most robust ...

Setting a New Standard in Safety Signal Analytics

ArisGlobal Announces the Launch of LifeSphere Clarity  As a pharmacovigilance ...

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ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 500 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.

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