Solutions

One platform, tailored to your industry

Every industry tests, reviews and reports differently. HDLIMS combines a unified platform with industry-specific workflows, terminology and compliance controls, so you start close to where you need to be.

Pharmaceutical QC

HDLIMS connects raw material testing, in-process control, finished product release, stability and environmental monitoring in one validated system, so QC stops being the bottleneck between manufacturing and market.

21 CFR Part 1121 CFR Part 211EU GMP Annex 11EU GMP Annex 1
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Biotech & Biologics

HDLIMS gives discovery, process development and QC teams one shared data model, so knowledge built at bench scale carries through tech transfer, and every GMP lot traces back to its cell bank, raw material lots and process parameters.

21 CFR Part 1121 CFR Parts 600–68021 CFR Part 1271EU GMP Annex 2
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Clinical & Diagnostics

HDLIMS handles the full specimen lifecycle for reference, molecular and clinical research labs, from requisition and accessioning through multi-step molecular workflows to signed reports delivered to the ordering provider’s EHR.

CLIA (42 CFR Part 493)CAP accreditationISO 15189:2022HIPAA
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Biobanking

HDLIMS tracks every specimen, aliquot and derivative from collection to distribution, linked to the donor’s consent, so your biobank can say exactly where a sample is, how it was handled and whether it may be used for a given study.

ISO 20387:2018ISBER Best PracticesNCI Best Practices for Biospecimen ResourcesSPREC
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Food & Beverage

HDLIMS connects plant QC labs, central labs and contract labs in one system, so holds, results and releases follow the same rules at every site, and your HACCP and food safety plans have verified data behind them.

FSMA (21 CFR Part 117)FSMA Section 204 traceabilityHACCPISO 22000:2018
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Environmental Testing

HDLIMS takes environmental samples from bottle order and field collection through login, batching, analysis and data review to client reports and EDDs, with holding times and batch QC enforced along the way.

ISO/IEC 17025:2017TNI StandardNELAP accreditation40 CFR Part 136
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Chemicals & Materials

HDLIMS runs the routine work of plant and product labs, from scheduled shift samples and grade-specific limits to live control charts and CoAs, and connects it to the historian and ERP your operations already depend on.

ISO 9001:2015ISO/IEC 17025:2017IATF 16949:2016AIAG PPAP
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Contract Testing Labs

HDLIMS runs the commercial and scientific sides of a contract lab together, from quote and sample receipt through testing, study reports and invoicing, while keeping every sponsor’s data segregated and every SLA in view.

ISO/IEC 17025:201721 CFR Part 58OECD GLP21 CFR Part 11
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Across every industry

What every HDLIMS solution shares

Industry solutions are configurations of the same platform, so you get specialization without fragmentation.

Industry templates

Start from preconfigured sample types, workflows, specifications and reports for your industry, then tailor without code.

Regulatory controls

Audit trails, electronic signatures and data integrity controls designed for GxP, ISO and clinical frameworks.

Connected ecosystem

Instruments, ERP, MES, EHR and customer systems connected through open APIs and proven integration patterns.

Multi-site ready

Harmonize methods and master data globally while keeping site-specific workflows, languages and permissions.

Don’t see your industry?

HDLIMS is configurable for any testing or research laboratory. Tell us about your workflows and we will show you how the platform fits.