LIMS Consulting and Laboratory Digital Transformation

We help laboratories move from paper forms and scattered spreadsheets to a traceable digital workflow for sample tracking, result approval and reporting. We are not tied to any software vendor.

Signs it is time to digitalise

  • Nobody can say at a glance where a sample is in the process
  • Results are retyped from instrument to form to report, with transcription errors
  • Spreadsheets with unclear versions and no validation
  • Long report turnaround and approval steps that cannot be traced
  • Finding a record for an assessor takes hours

What a LIMS digitalises

Sample management

Registration, barcode labels, chain of custody, work orders, workload allocation and due-date tracking.

Results and reporting

Instrument integration, automatic calculations, limit checks, multi-step approval and report generation.

Quality and resources

Equipment calibration and maintenance, chemicals and reference materials, staff competence records, control charts.

Data integrity

User authorisation, audit trail, backups and controlled data changes.

ISO/IEC 17025 and data management

Clause 7.11 requires the information management systems used for laboratory activities to be validated before use, protected from unauthorised access, changed only under control and safeguarded for data integrity. A LIMS project is therefore not just software installation — it is part of your quality management system.

Our LIMS implementation approach

  1. Needs analysis: current workflows, data flows and bottlenecks, reviewed on site.
  2. User requirements specification (URS): selection criteria and must-have functions in writing.
  3. Vendor evaluation: demo scripts and a technical and functional comparison of offers.
  4. Implementation project: configuration, master data (methods, parameters, limits), instrument integration and data migration.
  5. Validation: test scripts that verify functionality, with documented results.
  6. Go-live and training: user training and procedures updated for the new system.

Setting up a new laboratory? Planning the LIMS during laboratory setup avoids later data migration and process rework.

Deliverables

  • Workflow and data flow analysis
  • User requirements specification (URS)
  • Vendor comparison matrix and demo scripts
  • Validation plan, test scripts and validation report
  • Spreadsheet validation records
  • Updated procedures and user training records

Prepared by the Molar Çevre technical team · Last reviewed:

FAQ

Frequently asked questions

What is a LIMS?

A Laboratory Information Management System manages laboratory data in one place, from sample receipt to result approval and reporting — including sample tracking, workload allocation, equipment and calibration tracking, reporting and audit trails.

Do you sell LIMS software?

No. Our consulting is vendor-neutral: we define your requirements, help you compare systems, manage the implementation project and make sure the system is validated in line with ISO/IEC 17025.

Does a small laboratory need a LIMS?

Not always. It depends on sample volume, customer and reporting load and team size. For some laboratories, validated spreadsheets and good document control are enough. We make that call together during the needs analysis.

Do spreadsheets need to be validated?

Yes. ISO/IEC 17025 clause 7.11 requires software used to process laboratory data to be validated for functionality before use, and this includes in-house spreadsheets.

Let's map out the roadmap for your laboratory

Book a free initial consultation: we'll review where you are today and prepare a tailored work plan and proposal.

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