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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 connected system.

  • Manage everything within one system

  • Make it easy to show the story of your study to regulatory agencies

  • Expedite site selection by up to 35%

  • Reduce trial risk by over 75%

See How Inspection Readiness Works

Trusted By Organizations, Big And Small

Worldwide Clinical Trials
Galderma
Abbvie
CSL
MERZ
Eli Lilly
Daiichi-Sankyo
teva
Servier
BAUSCH+Health
BAUSCH + LOMB
endo
Menarini
eurofins

Trial Interactive

By The Numbers

10 M+

TMF Documents Processed


250 +

TMF Inspections Supported

(FDA, MHRA, EMA, PMDA)

250 +

Sponsor Clients Served

Trusted across all their trials

60 +

CRO Clients Worldwide

Using our system for all trials

15 K

Studies Managed Annually

Across global clinical trials

100 +

TMF's Rescued Mid Study

Reconciled under tight deadlines

Latest from our leadership

21 CFR Part 11
International Organization For Standardization (ISO)
SSAE 16 SOC 2 Type 2
Annex 11
GDPR
GAMP
HIPPA
HiTrust - CSF
Privacy Shield