ARCLIUM

ClinDOC™ · Clinical Document Optimization Consultant

The protocol changes.
What else needs to change?

Connect protocol requirements to supporting study documents—and give reviewers the evidence to assess alignment and amendment impact.

  • Keep the governing protocol and document versions in view.
  • Investigate potential inconsistencies and missing coverage.
  • Track amendment impacts, affected documents, and review decisions.
Request a ClinDOC walkthrough

Protocol first. Accountable human review throughout.

ClinDOC · Document review workspaceExpand ↗
ClinDOC · Document review workspace — actual application displaying synthetic study information
ClinDOC in the hosted demo · Synthetic study-document review.

Inside the product

From a changed requirement
to an informed review decision.

01 / ORIENT THE REVIEW

See what still needs attention.

Review requirement coverage, open confirmation items, document issues, and pending amendment actions across the selected study scope.

ClinDOC · Executive ReviewExpand ↗
ClinDOC · Executive Review — actual application displaying synthetic study information
Hosted demo · Requirement coverage and review work across seven synthetic studies.
02 / ASSESS THE IMPACT

Track each affected document.

  • Review the protocol event and changed section.
  • Identify affected documents and responsible functions.
  • Track pending, update-required, and completed dispositions.
ClinDOC · Amendment Change TrackerExpand ↗
ClinDOC · Amendment Change Tracker — actual application displaying synthetic study information
Hosted demo · Synthetic amendment impacts, document owners, and pending decisions.
03 / FOLLOW THE REQUIREMENT

Read the requirement-to-document connection.

Use the coverage matrix to connect a protocol requirement, responsible function, complementary document, evidence anchor, and review decision.

ClinDOC · Protocol-to-Document Coverage MatrixExpand ↗
ClinDOC · Protocol-to-Document Coverage Matrix — actual application displaying synthetic study information
Hosted demo · Synthetic requirement-to-document connections. Package classifications and human review decisions remain distinct.

Across study functions

One protocol.
Many connected documents.

  • Data management plans and completion guidelines.
  • Monitoring plans, laboratory manuals, and vendor specifications.
  • Medical, safety, and statistical plans.
  • Document versions, source connections, and review history.

Shown here: ClinDOC within the current hosted demo. Client integration, access controls, AI permissions, and validation are defined for each implementation. ClinDOC supports qualified review; it does not approve documents or make clinical decisions.

Start with your study

Show us where review
gets difficult.

Let’s discuss the expertise, review tools, or ongoing support your team needs.

Discuss your study
Product view

Synthetic demonstration. Select Close or press Escape to return.