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Simplify Requirements for Medical Devices with Regulatory Information Management Systems

Keeping track of all the information required to manage your ...

A Look Back at Partnerships in Clinical Trials Europe

By Danilo Pavlovic As both a conference attendee and ArisGlobal ...

If You’re a CRO, You’ll Want to Read This Success Story

As the outsourcing trend continues to grow, many biopharmaceutical and ...

A level playing field: Realizing the importance of emerging CROs

With declining R&D budgets, increased competition from larger CROs and ...

CRO (Contract Research Organization) Research & Development Trends

CRO industry grows as increasingly complex R&D trends demand advanced ...

Integration Paves the Way: Overcoming Clinical Challenges & Complexities

Clinical development challenges have never been tougher and more complex, ...

What is Really Required in a Modern EDC?

I wrote a post a couple of months ago about ...

Five Key Steps You Need For Trial Disclosure

Post by Mathias Poensgen First, it was mandatory to submit ...

The Challenge with Today’s Clinical Analytic Platforms

In today’s fast paced ‘all or nothing’ innovative solution-focused industry, ...

CRO Partners with ArisGlobal to Manage Clinical Trials

CUSTOMER BACKGROUND A full service contract research organization (CRO) specialized ...

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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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