Prepare sites
for activation.
Coordinate the distribution, collection and review of regulatory start-up documents, with visibility for study teams.
ALLYFE CLINICAL DOCUMENT PLATFORM
Manage the records.
Connect the teams.
Bring site start-up, eISF, eTMF and remote quality control into a modular environment for sponsors, CROs and research sites.
FROM SITE ACTIVATION TO DOCUMENT REVIEW
A shared workflow
for your trial documentation.
Coordinate regulatory document collection, review and follow-up across study teams. Use the modules that fit your workflow and connect document management with evidence review through CEE.
THE PLATFORM
Four connected capabilities.
Prepare sites
Organise documentation
at the site.
Manage investigator site files and document workflows, helping sites and sponsors coordinate outstanding actions.
Bring trial records
into one environment.
Organise trial master file documentation and support review of completeness, quality and timeliness throughout the study.
Review documents.
Coordinate follow-up.
Give authorised reviewers access to regulatory documentation so they can raise queries, leave notes and guide sites on next steps.
DOCUMENT MANAGEMENT + EVIDENCE INTELLIGENCE
Your records, organised.
Their meaning, connected.
The platform manages documents and workflows. CEE connects the evidence across those documents to surface potential gaps, contradictions and unresolved questions for expert review.
See CEE findings and supporting evidence →FIT THE WORKFLOW TO YOUR STUDY
Start with what
your team needs.
Choose your modules
Discuss the study processes and teams you need to support, from start-up to ongoing quality control.
Plan the connections
Review your existing systems and the integration requirements for your environment.
Define the rollout
Agree the scope, onboarding approach and review workflows before deployment.