Take control of compliance and deliver seamless inspections with IQVIA eTMF

IQVIA Technologies has an electronic Trial Master File that simplifies today's over-engineered products and implementations, empowering oversight without busting the budget.

Keep your studies on track and compliant

The IQVIA Electronic Trial Master File (eTMF) offers precision planning and intelligent automation to create and maintain an inspection-ready eTMF that you can count on. Its simple and intuitive design minimizes manual efforts and reduces risk.

Comparing eTMF solutions is complicated. We can help.

IQVIA Technologies provides an RFI/RFP template that sponsors of all sizes have used to select and evaluate the features that mean the most to them.

Get actionable insights into quality, timeliness, and completeness in real-time

See your customized dashboards and metrics upon login to get immediate insights into eTMF health. Understand and correct quality, completeness, and timeliness issues proactively for nonstop audit-readiness.

A practical approach to continuous eTMF compliance

IQVIA eTMF streamlines day-to-day TMF document workflows, quality control (QC) checks, and finalizations for your clinical operations. Guiding team members from task to task while maintaining detailed audit trails, IQVIA eTMF keeps everyone on the same page and always prepared for health authority inspections.

Study Set-Up Wizards

Quickly initiate new eTMF study environments with minimal clicks, guided by the eTMF study wizard.

Site Zone

Site-facing eTMF document exchange is simplified for site adoption with no additional integrations required.

eTMF Expert Services

IQVIA Technologies partners with your team and aligns resources to support eTMF document workflows, study-owner oversight, and eTMF DIA Reference Model quality assurance.

eTMF Archive

Remain inspection-ready beyond database lock and protect the huge investments made in completed trials. With simplified pricing independent of site volumes, IQVIA eTMF Archive drastically reduces the cost to comply with ICH GCP, FDA, and EMEA document retention requirements.