The Gene Box
Buyer's Guide

Lab Director technical scoping checklist

What to bring into a demo and technical scoping call - menu, LIMS webhook, brand files, sign-off path, and timing language already on the public site.

The Gene Box··5 min read

A technical scoping call is not a product tour. It is the session where a lab director, molecular pathologist, lab operations lead, and diagnostics BD decide whether a white-label interpretation layer can sit on the wet-lab and LIMS you already run - under your brand, with a qualified human on the report.

This checklist is the agenda for that call. Every item maps to a file or page already live: the laboratory proof packet, the weeks-scale scoping outline, and the API and white-label surface. Nothing here invents a certification, a customer logo, or a go-live date.

1. Who is in the room - and what they own

Bring the people who own the work, named the way the work is named:

  • Lab Director - the menu, the quality system, and what leaves the laboratory under your name
  • Molecular Pathologist - interpretation workload and the report that waits for qualified human sign-off
  • Lab operations - accession, report standardisation, and getting the file back into the LIMS
  • Diagnostics BD - partner-branded multi-omic offer for chains and hospital labs

If one of those seats is empty, someone else will guess - and the guess will break later. Put the missing owner on the calendar before you debate modules.

2. Laboratory context: menu under your brand

Ask (and answer) before demos scroll:

  1. Diagnostic laboratory or hospital lab?
  2. Which assays already run in-house - and which interpretation menus you want under your brand first?
  3. Who is qualified to sign a report today?
  4. Is the first wedge multi-omic interpretation (DNA, microbiome, blood read as one), clinical modules already on the platform (Clarity / Lens), or both?

Keep wellness modules off the default ask unless the laboratory requests them. Diagnostic-lab deployments lead with the interpretation layer, not a consumer kit story.

3. LIMS and webhook - sandbox first

The published integration path is REST and JSON, OAuth 2.0, a sandbox, and webhooks when a report is ready. HL7/FHIR R4-compatible exchange is described for EHR and LIS integration. Public endpoint families on the API page include /v1/samples, /v1/reports/{id}, microbiome routes, and blood overlay.

On the call, map:

  1. Accession identifier - what your LIMS already uses
  2. Webhook destination - where a report-ready event should land
  3. Sandbox - test before production keys (the API page: sandbox access day 1; production keys after onboarding)

Do not exchange production credentials on a first scoping call. The example webhook JSON in the proof packet uses public endpoint names. It is an illustrative schema for the conversation - not a production contract and not a credential.

4. White-label: brand files that must be real

White-label is not a logo pasted on a PDF. Confirm you can supply:

  • Domain (or subdomain) for the patient / practitioner surfaces
  • Logo, colour palette, typography
  • Report header, footer, and cover expectations
  • Language needs already listed publicly (English, Arabic, Turkish, and more)
  • Tonality by role - patient-facing vs clinician-facing depth

The sample partner-branded report in the proof packet is the layout under discussion. Open it, Print → Save as PDF. It is structure only: not a patient result and not a diagnosis. Do not forward it as either.

5. Sign-off and the decision-support boundary

State this boundary early:

Decision-support, not diagnosis - every interpretation traced to evidence and signed off by a qualified human. The ordering clinician stays responsible for the clinical conversation.

Ask the vendor (including us):

  1. Is a qualified human review recorded before a report ships?
  2. Where does each interpretation trace in the report a clinician can open?
  3. Is marketing language consistent with that boundary across site, deck, and contract?

Compliance line already published: ISO 9001:2015 certified · pursuing ISO 13485 · GDPR compliant. Cite it exactly. Do not invent CAP, NABL, or other marks that are not on the public site.

6. Timing language already published - not an SLA

Use only the sentences already on the public site:

PathPublished timingSource
RESTful API onboarding1-8 daysAPI page
White-label configuration7-8 weeksAPI page
Laboratory partnership cycle (incl. training / integration)3-6 monthsFAQ

Those are scoping inputs. They are not a contractual turnaround. The call sets the calendar. If a deck promises a go-live date before LIMS mapping and brand files are agreed, treat that as a red flag - including if it is ours.

7. Commercial scope without turning the page into a price list

Platform licensing plus a per-interpreted-report fee, from roughly $3-5 on top of the wet-lab you already run, is the public commercial frame. A written quote is produced from the call. This checklist is not a price list.

Ask what surrounds the headline number: setup, minimums, volumes you actually run, and exit terms for your accumulated report history. Bring your real volumes; do not model from brochure volumes.

8. Proof packet leave-behind (open these in the meeting)

FileWhy it is on the table
Laboratory proof packetIndex of the four files
Sample partner-branded reportLayout and brand structure
Example webhook JSONIllustrative LIMS event shape
Scoping outlineThis agenda in packet form
Compliance lineExact certification / decision-support wording

Nothing in the packet is a named customer, a revenue figure, or a clinical claim.

Closing

If you run a diagnostic laboratory and want the interpretation layer under your brand:

  1. Open the proof packet
  2. Book a demo and technical scoping with the seats above
  3. Read the diagnostic laboratories page for the conversion path

Building under your brand? Start at labs - then bring this checklist to the call.

FAQ

What should a lab director bring to a technical scoping call?

Menu under your brand, who signs reports, accession ID pattern, webhook destination, brand files (domain/logo/header/footer), and whether you want API-into-LIMS, white-label platform, or both. Use the published proof packet as the leave-behind.

Is “weeks not months” a service-level agreement?

No. The API page publishes RESTful onboarding in days (1-8) and white-label configuration in weeks (7-8). The FAQ publishes a laboratory partnership cycle in months (3-6). Those are scoping inputs. The call sets the calendar.

Does the interpretation layer diagnose?

No. Decision-support, not diagnosis - every interpretation traced to evidence and signed off by a qualified human. The ordering clinician stays responsible for the clinical conversation.

Keep reading

Building under your brand?

White-label interpretation for diagnostic laboratories. Decision-support, not diagnosis.