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In-house veterinary diagnostics

Veterinary Laboratory
Solution

Build your laboratory around the results your team needs.

Connect analyzer selection with your test menu, animal species, sample workload and ongoing supplies. Mevidon helps you define equipment, reagents and support requirements in a coordinated laboratory proposal.

Species & assay fitQuality-control planningLong-term supply scope
Illustrative clinical equipment composition including laboratory and endoscopy systems
Illustrative equipment composition · Final laboratory configuration is project-specific.

Define your starting point

Choose the service before the instrument.

For clinics starting in-house testing, hospitals expanding diagnostic capacity and laboratory project buyers. Decide which results your team needs on site and which tests remain with a reference laboratory.

Test menu & species

List required analytes, patient species and clinical departments. Identify assay limitations and the reference information needed for interpretation.

Volume & turnaround

Share average and peak sample numbers, urgent testing needs and available operators. Compare sample-to-report workflow, not instrument run time alone.

Space & ongoing resources

Review bench space, sample preparation, storage, waste handling, software and reagent-replenishment arrangements.

Testing capabilities

Turn your test menu into an equipment plan.

These groups provide a planning framework, not a requirement to purchase every instrument. Exact assays and supported species must be confirmed for each proposed model.

Hematology

Planned testing scope

CBC testing matched to the species and reporting needs of your practice.

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Confirm during selection

Species validation, differential requirements, sample volume, flags, smear-review workflow and quality-control materials.

Clinical chemistry

Planned testing scope

Chemistry testing selected around your required analytes and daily workload.

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Confirm during selection

Dry or wet format, panel flexibility, reagent handling, calibration, controls, waste and cost per reportable result.

Electrolytes & blood gas

Planned testing scope

Targeted testing for the services defined by your emergency, inpatient or anesthesia team.

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Confirm during selection

Measured versus calculated parameters, sample type, handling requirements, cartridge storage and operating environment.

Urinalysis

Planned testing scope

Urine-testing equipment and supporting sample-review processes.

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Confirm during selection

Species and method applicability, compatible strips or supplies, sample preparation and whether sediment examination is included or separate.

Coagulation

Planned testing scope

Selected hemostasis testing based on your clinical team's requirements.

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Confirm during selection

Available assays, specimen requirements, reagent and control supply, calibration and result-review procedures.

Immunoassay

Planned testing scope

Hormone, biomarker or other assays supported by the selected analyzer and test kit.

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Confirm during selection

Assay-specific species validation, units, reference information, reagent shelf life and quality-control requirements.

PCR / molecular testing

Planned testing scope

Molecular workflows planned around the exact assays your laboratory intends to perform.

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Confirm during selection

Extraction, reagents, controls, contamination management, workspace separation and interpretation expertise; a thermocycler alone is not a complete testing service.

Additional requirements: electrolyte analyzers, hemoglobin meters and compatible consumables. Confirm which results are measured, calculated or outside the selected system's scope.

A practical procurement decision

Dry or wet chemistry: compare the workflow.

Compare specific instruments at your expected workload. Neither format is automatically the best choice for every clinic.

Questions to compare before choosing a chemistry system
Planning factorDry / unit-use systemsWet chemistry systems
Purchasing focusConfirm the selected rotor, slide or cartridge system and available panels.Confirm analyzer capabilities, assay menu and compatible liquid reagents.
Workload fitAssess single-sample workflow, run capacity and panel use at your actual volume.Assess batch or random-access workflow, daily workload and reagent utilization.
Reagent costInclude panel price and unused analytes in the comparison.Include pack size, calibration, controls, dead volume and open-container stability.
Daily operationReview preparation, loading, storage, maintenance and waste handling.Review pipetting, reagent handling, water needs where applicable and maintenance.
Quality planningConfirm manufacturer instructions for controls and independent quality assessment.Confirm calibration, control materials, lot changes and quality-review procedures.
Supply continuityConfirm proprietary supply dependence, shipment conditions and replenishment lead time.Confirm reagent compatibility and validated alternatives; do not assume an open system.

From sample to report

Make quality part of the laboratory setup.

Document responsibilities and procedures across collection, testing and reporting. Equipment purchase is one part of a functioning laboratory.

Sample suitability

Confirm collection containers, sample type, preparation, volume and handling limits in the relevant instructions.

Quality control

Plan controls, calibration where required, maintenance logs and actions when checks fail. Have your laboratory lead set and review the quality plan.

Species & interpretation

Review species-specific validation, reference intervals, result flags and follow-up review procedures before clinical use.

Reporting & traceability

Confirm patient identification, units, reference information, result review and transfer into your hospital or laboratory information system.

Quality planning resources are available in the ASVCP laboratory guidelines. Built-in instrument checks should not be assumed to replace a complete quality-management program.

Supply continuity

Plan the next reagent order before the first.

Discuss consumables alongside the analyzer, especially where a platform depends on proprietary rotors, cartridges or kits.

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Compatibility & order quantities
List compatible reagents, controls, calibrators, cleaning materials and collection supplies. Confirm packaging and minimum order quantities.
Storage & useful shelf life
Review shipping temperature where relevant, storage requirements, expiry at delivery, open-pack stability and expected consumption.
Replenishment & disruption planning
Agree lead-time estimates and reorder planning. Identify reference-laboratory or other contingency arrangements for supply gaps or downtime.

Total operating cost

Compare cost per reportable result.

Use a consistent time period and test definition across proposals. A panel and an individual analyte are different units of comparison.

Direct testing costs

Reagents, cartridges, controls, calibrators, sampling supplies and other required consumables.

Utilization & waste

Repeat runs, expired material, partially used packs and unused panel capacity at your real workload.

Laboratory overhead

Allocated service, maintenance, software, staff time and equipment costs, kept visible in the comparison.

A consistent comparison method

Cost per reportable result = total attributable costs for the period ÷ reportable patient results for that period. Record assumptions about testing volume, repeats, waste and included overhead.

Grow with your workload

Build capability in practical stages.

  1. Stage 1 · Core service

    Establish routine testing.

    Prioritize the agreed test menu, sample preparation, controls and operator training. Keep a defined referral pathway for tests outside your scope.

  2. Stage 2 · Capacity

    Address actual bottlenecks.

    Use workload and turnaround records to decide whether more capacity, better reporting integration or an additional test service is justified.

  3. Stage 3 · Specialist testing

    Add assays with a complete plan.

    Evaluate molecular or other specialist testing with the necessary workflow, staff expertise, assay validation and sustained supplies.

Working with Mevidon

Agree the scope from selection to handover.

Mevidon is a veterinary medical equipment manufacturer and one-stop supplier. Confirm the following deliverables for your laboratory project.

  1. Review the laboratory brief

    Discuss test menu, species, sample volume, operator resources and existing instruments.

    Agree: the proposed analyzer and supply list.
  2. Confirm configuration & costs

    Review assays, accessories, software, documents, reagents, storage and commercial terms.

    Agree: inclusions, exclusions and replenishment scope.
  3. Prepare delivery & setup

    Confirm bench, utility and environmental requirements, agreed inspection records and shipping arrangements.

    Agree: preparation tasks and delivery documents.
  4. Handover & ongoing support

    Define operation guidance, maintenance, service contacts and model-specific warranty arrangements.

    Agree: acceptance checks, training and support scope.

Clinical validation, quality policies and result interpretation remain with qualified laboratory professionals. On-site service and special shipping conditions require separate confirmation.

Illustrative planning example

A clinic starting in-house diagnostics.

This is a planning example, not a customer installation or a fixed equipment recommendation.

Starting requirement
A small-animal clinic wants selected routine results on site while retaining referral testing for less frequent assays.
Selection discussion
Compare the actual hematology, chemistry and urinalysis workload with preparation time, control costs and reagent utilization.
Planning outcome
An initial equipment and supply list, a quality-management responsibility plan and a staged review of further testing capabilities.

Laboratory procurement FAQs

Clarify the details before ordering.

Answers for clinic owners, laboratory teams and international equipment buyers.

What equipment is needed for an in-house veterinary laboratory?

Start with your test menu, species and workload. Discuss hematology, chemistry and urinalysis, then add other systems when the intended service justifies them. Include sample preparation, quality control, storage and reporting.

Should we choose dry or wet chemistry?

Compare your actual volume, required analytes, staffing and reagent usage. Evaluate calibration, controls, expiry-related waste and maintenance along with instrument cost. Suitability depends on the specific systems, not the format alone.

Can one analyzer test every animal species?

Do not assume this. Confirm validation for the intended species and assays, reference information, sample requirements and limitations. A species selection in software does not by itself demonstrate analytical suitability.

How much sample does the analyzer need?

The required volume depends on the model and test. Confirm sample type, collection container, aspiration volume, dead volume and preparation requirements from the current instructions for the selected configuration.

How do we calculate the real cost per test?

Include reagents, controls, calibrators, consumables, repeat runs, discarded expired material and allocated service costs. Divide by reportable patient results for the same period; compare panels and individual tests consistently.

Can Mevidon supply reagents and consumables after the initial purchase?

Discuss compatible reagents, controls, calibrators and supplies with the equipment quotation. Confirm available products, order quantities, storage conditions, shelf life at delivery and replenishment terms for your destination.

Does built-in quality control replace external controls?

Do not assume it does. Review what the built-in checks actually assess and develop a documented quality plan with your laboratory lead, following manufacturer instructions and relevant veterinary laboratory guidance.

Can results connect to our hospital or laboratory software?

Integration depends on the analyzer, software version, interface and receiving system. Confirm export formats, interface licenses, patient identification, units and a practical transfer test before agreeing compatibility.

Is a PCR machine enough to start molecular testing?

No. Define the assay workflow, including sample preparation or extraction, validated reagents, positive and negative controls, contamination management, trained staff and result interpretation. Confirm all required components before ordering.

What installation and training support is included?

Confirm setup guidance, operation training, maintenance instructions and troubleshooting arrangements in the quotation. On-site service, travel, warranty and parts are model- and destination-specific; clinical validation remains with qualified laboratory professionals.

Start your laboratory project

Share your test menu and workload.

Send the details you already know so we can discuss an equipment and supply proposal.

  • Country, facility type and animal species
  • Required tests and average / peak sample volume
  • Turnaround needs and available operators
  • Existing analyzers, software and storage conditions
  • Budget priorities and purchasing schedule

Email your test menu or equipment list to tuxiaohong63@gmail.com with your project reference.

Planning multiple departments? Explore our new veterinary hospital solution. Final models, documents and support scope are confirmed in the quotation.

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