Modernize Clinical Trial Processes

Enable active TMF management and oversight for real-time inspection readiness, visibility, and control.

Recent survey findings show a significant increase in the adoption of modern purpose-built eTMF applications.1 This enables organizations to automate processes, manage documents in real-time, and achieve active trial management — ultimately improving inspection readiness.

Why the Industry Is Transitioning Away From Paper

Enable remote work across teams

Reduce clinical operations risk

Enhance collaboration with development partners and CROs

Gain actionable insights for proactive trial decisions

Achieve an ongoing state of inspection readiness

Increase speed and quality of clinical trials

Optimize TMF Management

As new inspection approaches and digital, decentralized trial approaches gain ground, now is an ideal time to move from paper-based processes to electronic TMF systems. Learn how to improve inspection readiness and reduce trial timelines.

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eTMF Success Stories

ALVOTECH TRANSITIONED FROM PAPER TO SPONSOR ETMF

Alvotech improved inspection readiness by replacing a paper-based process for sponsor-managed documents.

CANCER RESEARCH UK MODERNIZES CLINICAL TRIALS

CRUK replaced a paper eTMF to drive efficiencies and improve quality.

NESTLE ENHANCES CRO COLLABORATION WITH TMF TRANSFER

Nestle improved inspection readiness and collaboration with CRO partners with streamlined transfer of TMF documents.

Access industry best practices and guidance to stay inspection-ready and watch more customer stories.

Streamline Processes with Vault Clinical Suite

Next Steps



1. Veeva Systems, “Unified Clinical Operations Survey Report”, veeva.com, 2020.