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Smart ICSRs: Digitalizing Case Processing

Opportunities for Improved Safety Data Collection from PSPs

Leveraging an IDMP Enabled Platform for Regulatory Transformation

How Medical Affairs is Becoming a Strategic Pillar in Pharma

Science and data are transforming the groundwork for pharma for ...

A CRO’s Journey to eTMF

Exploring the Benefits of CTMS Automation

Video Description

Journey to IDMP and Beyond

Regulatory teams serve as a gateway between life science organizations, ...

Electronic Trial Master File (eTMF) Systems Tell Compelling Story of COVID-19 Vaccines

The rapid development of Covid-19 vaccines may lead more drug ...

Balancing Speed, Safety, and Risks in a Global Pandemic

In the age of Covid-19, the cause of a global ...

Top 5 Reasons Why LifeSphere Clinical Trial Management System Works for CROs

Working in clinical operations at a small or midsized Clinical ...

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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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