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How Clinical Operations Can Accelerate Through De-risking Clinical Trials

Advances in clinical trial design and technology are significant contributors ...

How to Ensure a Full-Proof IDMP Strategy in 3 Steps

Robin Schilling, Product Manager for LifeSphere IDMP, discusses the core ...

Staying Ahead of ICH E6(R3) Good Clinical Practice Guidelines

Modernization is critical to enhance patient experience and boost clinical ...

COVID-19 and Vaccine Safety Brings Pharmacovigilance Center Stage

The public is more aware of drug safety and health ...

The Risks and Rewards of Decentralized Clinical Trials

DCTs completely revise historical trial processes by executing trials through ...

How RIMS Help Manage Increasing Complexity in Regulatory Affairs

Managing the submission of medicinal products, medical devices, and biologics ...

Benefits of Integrating Your Medical Information and Safety Workflows

Data is the lifeblood of businesses today. Data informs strategy ...

Synergy and Efficiencies Within: The Benefits of a Connected Clinical Platform

Change is the lone constant you can depend on. When ...

To Prepare for IDMP, Organizations Must Think Years Ahead – Not Months

When selecting an IDMP solution, remember decisions made today will ...

Key Features of eTMF Systems for Clinical Trial Success

Why Having a Well-Prepared eTMF is Important A well-prepared Electronic ...

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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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