AureqoLab · laboratory workflow software

From submission to reviewed results and CoAs.

For smaller, private analytical laboratories managing customer submissions, samples, manually recorded results, review and Certificates of Analysis.

In active development. Explore the current workflow using demonstration data; any pilot is discussed separately.

Current pilot focus

A workflow for research peptide sample testing.

The current AureqoLab pilot solution is built around laboratories testing research peptide samples. It connects the client’s test request with sample records, manually entered results and scientific review. Aureqo supplies software, not laboratory testing services. Your laboratory performs the testing and remains responsible for scientific review and approval.

After an authorised scientist approves the results and issues the certificate, AureqoLab generates and stores the Certificate of Analysis (CoA) PDF, retains its record and version history in the database, and queues an email notification for the requesting customer organisation. Clients can sign in to access the issued CoA.

Have a different workflow? Enquire about a custom solution for your laboratory. We are happy to work through your requirements, assess feasibility and agree a separate build fee, deliverables and milestones before development begins.

Follow the submission through review and issue.

Keep the customer request, sample, manually recorded result revision and review decision connected to the issued certificate. The laboratory remains responsible for the scientific work and its interpretation.

AureqoLab covers a focused LIMS-style workflow. A full LIMS, instrument integration, automated result import and scientific calculations are outside the current scope.

Inside the workflow

From incoming work to controlled output.

These views reflect implemented AureqoLab structures and use demonstration records only. They are interface illustrations, not a live application session.

01 · Workload visibility

See the queue before work becomes a hand-off problem.

Laboratory staff can see submitted samples, work in progress, pending review and results ready for issue in one operational view.

02 · Sample progression

Keep each requested test connected to the sample.

Submission context, receipt, structured results and review state move together through an explicit workflow rather than separate spreadsheets.

03 · Review and issue

Issue from the approved result revision.

Certificate preview, approval state and controlled issue remain tied to the result record. Issued versions are preserved rather than silently replaced.

Product preview

What the current development covers.

AureqoLab is in active development. The areas below reflect the current product direction and implemented workflow surfaces, not a promise of general availability.

Implemented workflow areas

  • Submission management
  • Sample lifecycle
  • Structured test results
  • Scientific review
  • Certificate generation and revision history
  • Audit history

Validation and scope boundaries

Operational readiness and pilot arrangements remain under validation. Current scope does not include a configurable workflow engine, full quality management, equipment management or automated instrument integration.

Establish the product fit

Bring one workflow you want to improve.

Use the walkthrough to compare your submission, manual result entry, review and certificate process with the current product. We will identify gaps and discuss whether a separately scoped pilot is useful.

The current product follows a focused workflow. We are happy to discuss custom solutions for your laboratory; additional stages, forms or integrations require an explicit scope and feasibility assessment.

Request a product walkthrough
From interest to evaluation

A clear next step.
A pilot only if it fits.

A walkthrough starts the conversation. It does not commit your laboratory to a pilot, a subscription or a system change.

  1. Choose one process

    Bring your submission, manual result entry, review and certificate process. Describe the problem without sharing confidential laboratory records.

  2. See the current software

    Walk through demonstration data. Compare the product with your process and identify what fits, what is missing and what falls outside its scope.

  3. Assess a scoped pilot

    If there is a useful fit, discuss a paid pilot. Agree the scope, fee, duration, responsibilities and success criteria separately, including any custom build work, before the pilot begins.

Before using laboratory data
Data handling, access, support, recovery and exit arrangements need to be assessed and agreed. Products remain in active development; pilot availability is not guaranteed.

Request a product walkthrough
A focused starting point

Reduce the gaps between systems and hand-offs.

Review indicative AureqoLab pricing or discuss how the workflow fits your laboratory. AureqoLab supports operational traceability without claiming to replace accreditation, quality systems or scientific judgement.

Request a product walkthrough