LiveTMF is coming to Trial InteractiveRead it

A regulator never sees your study. They see the file.

LiveTMF knows every document your trial owes, as of today or any past date, and cites the regulation behind each one.

The problem

Every trial has an expected document list. Almost nobody trusts it.

The list is set up once, at study start. Then sites activate, protocols amend and investigators change, and the list falls behind. Teams reconcile the gaps by hand, often just before an inspection.

CTMS

A new principal investigator joins a site

+5 owed· +1 later

Regulatory

The sponsor releases a protocol amendment

+24 owed

Safety

A SUSAR becomes an IND safety report

+1 owed· +21 later

Obligations LiveTMF derived in one week of its demo study.

LiveTMF

The file, understood.

Explore LiveTMF

Always current

The document list recomputes when the study changes.

Any past date

The file as it stood on any day you pick.

Explained and cited

Every gap traced to the regulation behind it.

The LiveTMF study dashboard

Why VDC

Trust is everything.

The file is what a regulator judges, so the software behind it has to earn its place.

In production today

Delphi is live in production with Veeva.

Our document intelligence product classifies clinical documents and extracts their metadata, then hands the results to your eTMF for approval. Delphi fills the file. LiveTMF understands it.

Explore Delphi

99%+

classification and extraction accuracy

1M+

documents a year per instance

50+

languages supported

SOC 2 Type 2, tested and attested by Prescient Assurance

Security

SOC 2 Type 2 audited

Tested and attested by Prescient Assurance.

Supports

  • 21 CFR Part 11
  • EU Annex 11
  • HIPAA
  • GDPR