Professional review

Qualified people remain accountable for what reaches you.

The platform organises sources, evidence and conflicts. It does not replace professional judgement or turn a rule result into an automatic recommendation.

Laboratory professional preparing a microplate for controlled analysis
01Verified sample
02Quality controlled
03Human reviewed

Genetics interpreted alongside current health context

Consent & provenanceEvery permission and source version recorded

Qualified reviewSafety and context checked before release

Measured, not imaginedNo diagnosis or deterministic prediction

01

Review is assigned by scope

A dietitian reviews every action plan. A medical reviewer, pharmacist, genetic counsellor or second reviewer is added when the case, finding or safety rule requires their scope.

  • Role and active assignment both required
  • Unrelated case data stays hidden
  • Break-glass access is exceptional and audited
02

Reviewers see provenance—not a mystery score

The workspace shows the source, date, questionnaire version, customer edits, laboratory version, evidence item, rule output and clinically relevant changes behind each candidate finding.

  • Original customer wording retained
  • Restricted notes receive stricter access
  • Material changes are highlighted
03

Conflicts must be resolved explicitly

Pregnancy, allergies, medicine interactions, major renal or hepatic context, active treatment, abnormal biomarkers or insufficient evidence can block or qualify a finding regardless of the genetic association.

  • Hard blocks cannot be dismissed silently
  • Missing current context can replace an action with a test or clinician question
  • Second review required for defined high-impact cases
04

Decisions are structured and signed

A reviewer can approve within policy, limit, suppress, request more information, refer or hold. The decision stores the reason, role, timestamp, e-signature and source versions.

  • No free-form “admin approved” toggle
  • Clinical hold stops report release
  • Every override requires an approved reason
05

Your plan stays focused

The final action plan contains no more than three customer priorities unless an authorised override is recorded. Food and lifestyle appear before optional product considerations.

  • Customer goals and feasibility guide prioritisation
  • Genetics alone never creates a product or dose
  • Medication decisions stay with the treating professional
06

Corrections remain visible

If a reviewer, laboratory or customer corrects material source information, the affected interpretation is reassessed. A new report version is created and the prior version remains in the audit chain.

  • Reason for change explained
  • Affected actions can be paused
  • Customer receives a secure correction notice

Ready when you are

Start with a short suitability check.

It takes a few minutes, does not require payment, and confirms whether the service scope and supervised collection model fit what you need.

Service information is versioned and distinguishes measured findings, supporting evidence, personal context, professional judgement and limitations.