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IDMP, Key Engine to a Regulatory Strategy

Decentralized Clinical Trials – Collaboration Urgency Grows

ArisGlobal LifeSphere eTMF Boosts Collaboration in Clinical Research by Supporting New Trial Master File Standard

MIAMI, FL June 3, 2021 – ArisGlobal, the leading provider ...

The Unified Future of Regulatory Platforms

LifeSphere Medical Affairs Key Benefits

Chatbots: The World of Virtual Assistants and Their Opportunities in Medical Information

Digital Tools for Improved Stakeholder Engagement

5 Key Takeaways From the 2021 DIA Medical Affairs and Scientific Communications Forum

The DIA Medical Affairs and Scientific Communications (MASC) Forum is ...

LifeSphere Regulatory Key Benefits

LifeSphere Electronic Trial Master File (eTMF) System Brings New Efficiency to Contract Research Organizations (CROs)

Contract Research Organizations (CROs) have been enthusiastic early adopters of ...

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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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