Software for Analytical Laboratories
LIMS that were built for pharmaceutical giants don't fit the workflow of independent testing labs. You need systems that match how samples actually move through your floor.
Built for Analytical Labs, Not Adapted for It
Most Laboratory Information Management Systems (LIMS) were designed for large pharmaceutical companies with dedicated IT teams and compliance officers. Independent analytical labs face different pressures: faster turnaround demands, equipment sharing between clients, variable sample matrices, and strict accreditation requirements without enterprise-scale staff. Generic LIMS要么over-engineer every workflow or under-engineer critical ones like chain-of-custody and instrument integration.
Sample login still relies on spreadsheets that get overwritten or lost
No automated calculation of duplicate injection precision or linearity criteria
Instrument data sits siloed in vendor software instead of flowing into reports
Accreditation audits require manual assembly of raw data and calculation workbooks
Capabilities Built for Analytical Labs
Purpose-engineered features that address your industry's specific operational challenges.
Sample Tracking with Chain-of-Custody
Barcode-driven sample login with timestamped custody logs. Know exactly who handled each sample, when, and what action was taken.
Method & Template Management
Configure test methods (USP, IP, ASTM) with built-in calculation templates for potency, purity, dissolution, and stability studies.
Instrument Data Integration
Connect HPLC, GC, UV-Vis, and dissolution testers via standard data formats. Eliminate manual transcription errors and double-entry.
Automated COA Generation
Generate Certificate of Analysis templates that pull calculated results directly from instrument data. Digital signatures and PDF export included.
Audit-Ready Reporting
One-click assembly of raw data packages for NABL, ISO 17025, or FDA audit trails. Calculation workbooks auto-generated from method templates.
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Lab Instrumentation & Regulatory Experience
We've worked with analytical labs running USP-compliant potency testing and ISO 17025 accredited quality control. Our LIMS templates encode real-world calculation rules — duplicate injection %RSD, system suitability criteria, and stability study timelines — not textbook formulas. Every workflow decision is grounded in how samples actually move through your floor.
Frequently Asked Questions
Common questions about building software for Analytical Labs.
01Does this support FDA 21 CFR Part 11 compliance?
02Can it connect to our existing HPLC software?
03How do you handle method validation and version changes?
04What's the typical implementation timeline?
Get a free system audit for Analytical Labs
Get a free 30-minute audit of your current systems with specific recommendations for Analytical Labs workflows. No obligation.