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INDUSTRY SOLUTIONS

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.

1

Sample login still relies on spreadsheets that get overwritten or lost

2

No automated calculation of duplicate injection precision or linearity criteria

3

Instrument data sits siloed in vendor software instead of flowing into reports

4

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.

Feature 01

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.

Feature 02

Method & Template Management

Configure test methods (USP, IP, ASTM) with built-in calculation templates for potency, purity, dissolution, and stability studies.

Feature 03

Instrument Data Integration

Connect HPLC, GC, UV-Vis, and dissolution testers via standard data formats. Eliminate manual transcription errors and double-entry.

Feature 04

Automated COA Generation

Generate Certificate of Analysis templates that pull calculated results directly from instrument data. Digital signatures and PDF export included.

Feature 05

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.

PROVEN RESULTS

Case Study: Sohman Analytical

Industrial Instrumentation Manufacturer3 Weeks Sprint

A lightning-fast B2B catalog that loads in under 420ms and quadrupled organic search traffic in 90 days.

Sohman Analytical converted a slow, forgotten industrial website into a high-speed inbound lead engine that dominates technical search queries.

First-Page Search Rankings & 185% Inbound Lead Growth
<420ms
Page Load Time
Global median first contentful paint
99/100
Lighthouse Score
Flawless score across Performance, Accessibility & SEO
+340%
Organic Search Lift
Indexed keyword rankings increase within 90 days
THE SWEDANA DIFFERENCE

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?
Yes. We implement electronic signatures, audit trails, and version-controlled method templates that meet 21 CFR Part 11 requirements for electronic records.
02Can it connect to our existing HPLC software?
We build custom parsers for major instrument vendor formats (Agilent, Waters, Shimadzu). Data flows directly into the LIMS without manual export/import steps.
03How do you handle method validation and version changes?
Methods are version-controlled with full change history. When USP or internal method revisions occur, new versions are validated separately while historical results remain linked to their original method version.
04What's the typical implementation timeline?
A production LIMS with instrument integration and COA templates typically takes 10-14 weeks. We run bi-weekly sprints with weekly demos so you see working software early.
LIMITED SPRINT CAPACITY

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.

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