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Break through the complexity of global
clinical operations
regulatory compliance
inspection readiness
operational oversight
content management
site collaboration
study team & site training
quality management
site activation

See how our award winning eClinical platform and expert TMF Services reduce operational friction and accelerate innovation.

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Experience Award-Winning Technology

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The Enterprise Path to Inspection Readiness

Create, review, and archive clinical content. Launch compliance focused training. Index all required records in the eTMF

  • All within one system

  • Make it easy to show the story of your study to regulatory agencies.
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From site identification to close-out, clinical document processes and operational oversight are complex. Our electronic trial solutions simplify your clinical operations: expedite timelines, enable collaboration, improve quality, capture the full story of study, and pass inspections.

eTMF and TMF Services

Speed, scalability, peace of mind: Get industry-leading technology and/or services and stay inspection-ready.

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Content Management

Centralize your document collaboration and management from creation to archival in the eTMF.

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Trial Management

Speed site activation and improve oversight with remote site monitoring and mobile-first CTMS.

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Learning Management

Reduce risk with remote site and study personnel training. Automatically index training records in the eTMF.

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Trusted By Organizations, Big And Small

Worldwide Clinical Trials
Galderma
Abbvie
MacroGenics
CSL
Clinipace
MERZ
Avidity
PTC
axsome
SURROZEN
aura
Client Logo - 14 - Akebia
teva
Servier
ProTrials
BAUSCH+Health
BAUSCH + LOMB
endo

“Trial Interactive has helped us enable a critical piece of remote trial management: visibility into all documents needed to remotely oversee a clinical trial. We only touch documents once because documents flow seamlessly between GlobalLearn, the eISF, and the eTMF. With Trial Interactive, we help studies lower risk and achieve near real-time oversight, without site visits.”

Penelope Manasco, MD, CEO, MANA RBM

“We were up and running in two weeks with Trial Interactive. This also coincided with a 48-hour MHRA approval after final protocol submission, Our CRO/Sponsor team and partnership with Trial Interactive made it possible to expedite this critical, time-sensitive research.”

Thomas Ogorka, Founder and CEO, Orphan Reach

“Web based portal solutions have been identified as a critical imperative for achieving new gains in adverse event management efficiency. Our collaboration with Trial Interactive has produced a fully compliant safety portal platform to enhance workflow efficiency. We believe this is a breakthrough approach our respective client base will find compelling under a wide variety of applications.”

Michael O'Gorman, President and General Manager, Sentrx

"They get all the little details of the work that we do."

Senior Director, CRO

Latest from our leadership

Webinar

Ask an Expert TMF Series: Risk Proportionate Oversight That Works

Join Gill Gittens and Laurel Ann Schrader for a practical session on risk proportionate oversight in the TMF. Learn how to move from blanket review to focused checks that protect patient safety, data integrity, and inspection readiness.

Blog

AI in Clinical Trials: From Webinar Insights to Audit-Ready Implementation

Over three weeks, my colleagues and I hosted a webinar series on AI in clinical trials. The engagement shocked us: when we polled attendees in our final session, 50% reported already using AI in daily operations. This technology has moved from theory to operational reality faster than anyone predicted. 

Webinar

Study Startup Best Practices: Kickoff Meeting

The TMF is evaluated at inspection, but its success is determined at the kickoff meeting. This is where expectations are set, ownership is established, and the foundation is laid for a Trial Master File that must hold up from study start through final inspection.