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A Translyx product · Built on Privexa

Reviewer-gated synthetic control arms, ready for submission

Privexa Trace structures synthetic control arm workflows with reviewer sign-off, manual benchmark comparison, lineage, and submission-oriented packaging — for biotech, pharma, CRO, and clinical trial teams.

Built for

Clinical Sponsors

Biotech and pharma teams running evidence reviews and SCA programmes

CROs

Contract research organisations managing reviewer-gated trial workflows

Academic Groups

Research teams needing governed synthetic control arm methodology

Clinical Trial Offices

Teams responsible for evidence packaging and submission preparation

Built for teams that require a defensible audit trail

Privexa Trace covers the complete synthetic control arm workflow — from workup definition to reviewed output — with mandatory reviewer sign-off at SCA generation, manual benchmark comparison throughout, and submission-oriented packaging at every stage.

Every decision point is visible. Every output carries its lineage. The workflow does not abstract away the steps that reviewers and regulators need to see.

Product hierarchy

Translyx

Clinical technology holding entity focused on enterprise-ready, clinically credible healthcare AI.

Privexa

Field-level AI data protection layer. Sensitive healthcare data never leaves your environment.

Privexa Trace

Reviewer-gated synthetic control arm workflows with lineage, comparison workspace, and submission packaging.

BiotechPharmaCROClinical trial officeReview & governance

Workflow

The eight-step Privexa Trace workflow

Structured to move from workup setup to reviewed evidence output without hiding the decision points that matter.

1

New Workup

Initiate a structured workup for a specific clinical question.

2

Define Question

Articulate the research question, target population, and key parameters.

3

Find Comparables

Identify comparable historical and real-world datasets for cohort construction.

4

Dataset Fit

Assess dataset suitability, coverage, and alignment with the target question.

5

Cohort Builder

Build treatment and control cohorts with specialist review at each stage.

6Gate

Diagnostics & Review

Run diagnostics and complete reviewer sign-off before SCA generation.

7

SCA Analysis

Generate reviewed synthetic control arm analysis with visible lineage.

8

Submission Package

Export a submission-oriented package with methods, limitations, and provenance.

Comparison model

Three comparison paths inside one governed workflow

Trace is strongest when the comparison model is explicit: specialist-built manual arms remain visible, synthetic output is reviewed rather than assumed, and the final package carries all context forward.

Manual treatment arm

Specialist-entered benchmark representation of the treated population or reference treatment context. Built and reviewed before any synthetic generation.

Manual control arm

Specialist-entered benchmark control context used to assess workflow logic and comparability. Reviewed alongside the treatment arm.

Synthetic workflow output

Reviewer-gated synthetic output connected to diagnostics, lineage, and visible limitations. Not presented as a replacement for the manual arms.

Manual and synthetic comparison

Privexa Trace is not a replacement for specialist clinical judgment. Manual treatment and control arms remain central to the workflow — the synthetic output is assessed alongside them in the same governed environment, under the same reviewer accountability.

That structure produces stronger evidence packages: the benchmark remains visible, the synthetic construction is reviewed, and the final output carries both in context.

Worked example

1

A clinical team defines the question and target setting.

2

A trial specialist builds a manual treatment arm and a manual control arm.

3

Trace organises comparable evidence, dataset fit, and cohort construction.

4

Diagnostics and reviewer sign-off are completed before SCA generation.

5

The resulting package preserves lineage, limitations, and reviewed context.

Governance model

Governance built in, not bolted on

Reviewer gates, lineage, and visible limitations are not optional modules. They are structural features of how Privexa Trace operates.

Reviewer sign-off before SCA generation

Privexa Trace preserves a hard governance gate before any synthetic analysis can be generated. Statistics do not outrun human review.

Traceability and lineage

Each stage is structured so teams can follow exactly how evidence, cohort choices, and outputs connect through the workflow.

Visible limitations

Residual assumptions and workflow constraints stay visible rather than being hidden behind a polished output. Honest about current boundaries.

Submission-oriented packaging

Trace brings methods, reviewed decisions, provenance, and package-ready output into one coherent workflow — not an afterthought.

Honest scoping

What Privexa Trace includes — and what it does not

Included

  • Reviewer sign-off gate before SCA generation
  • Manual treatment arm entry and comparison
  • Manual control arm entry and comparison
  • Synthetic workflow output with lineage
  • Visible limitations in every output
  • Submission-oriented packaging
  • Audit trail across all workflow stages
  • Traceability of cohort construction decisions

Not included

  • Fully automated regulatory submission
  • Implied FDA, EMA, or Medsafe endorsement
  • Black-box output without reviewer gate
  • External patient data storage
  • Guaranteed regulatory acceptance

Regulatory posture

Designed to support submission packaging — not to claim regulatory approval

Privexa Trace is designed with the intent of supporting FDA, EMA, and Medsafe submission packaging workflows. It structures evidence with the discipline those processes require. It does not claim, imply, or guarantee regulatory acceptance of any output.

FDA-aligned workflow intent
EMA-aligned workflow intent
Medsafe NZ context

Common questions

Does Privexa Trace claim regulatory endorsement?

No. Privexa Trace is designed to support submission-oriented packaging and reviewer-gated governance workflows. It does not claim or imply regulatory endorsement from FDA, EMA, Medsafe, or any other body. All outputs carry visible limitations.

What data residency options does Privexa Trace support?

Privexa Trace is designed with data residency in mind for New Zealand and regional deployments. Integration and export options include SAS/R-compatible outputs and audit log exports. Contact Translyx for specific infrastructure requirements.

What is the difference between the manual arms and the synthetic output?

The manual treatment arm and manual control arm are specialist-entered benchmark representations. The synthetic workflow output is a reviewer-gated statistical construction. Trace keeps all three visible in one governed environment so they can be compared, not substituted.

See Privexa Trace in detail

Schedule a walkthrough of the eight-step workflow, reviewer gate model, comparison workspace, and submission-oriented output — with the Translyx team.