Pharmaceutical GMP Lyophilization

Lyopharm Tech freeze dryer models

GMP pharmaceutical freeze dryers for peptides, sterile injectables and biologics, with shelf areas from 0.5 to 5.4 m2 and validation-ready controls.

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Complete product range

5 traceable models for pharmaceutical gmp lyophilization

Open any model for its manufacturing reference and published engineering data.

Model comparison

Compare all 5 capacity points

Published values are a planning reference. Confirm the product or formulation, loading format, endpoint, utilities and complete cycle before purchase.

ModelReference capacityLoading formatCondenserBest fit
LPT-050S0.5 m2 shelf areaPilot vial loading<= -85 CClinical, peptide and process-development batches
LPT-100S1.0 m2 shelf areaPilot / small production<= -85 CSterile injectables and biotech production
LPT-200S2.16 m2 shelf areaProduction vial loading<= -85 CCommercial peptide and injectable lines
LPT-360S3.6 m2 shelf areaConfigurable shelf countMatched production condenserMedium-scale commercial fill-finish
LPT-500S5.4 m2 shelf areaLarge production loading<= -85 CHigh-capacity regulated production

Commercial confidence

What is defined before an order moves forward

No invented stock, delivery date or universal performance promise. The commercial file connects the machine to an approved technical basis.

01

Traceable model identity

Lyopharm Tech / SJIA manufacturing platform remains visible from quotation and technical agreement through manuals, spare parts and service.

02

Approved specification

Capacity, utilities, interfaces, options and acceptance conditions are recorded before manufacturing release.

03

Factory acceptance

The agreed FAT scope can cover dimensions, controls, alarms, refrigeration, vacuum and documentation checks.

04

Export and delivery plan

Packing, shipping terms, lead time, installation access and site responsibilities are confirmed in the quotation.

05

Commissioning support

Remote support is standard; qualified projects can include on-site installation, commissioning and operator training.

06

Warranty and spare parts

Warranty scope, exclusions, service route, consumables and recommended spare parts are stated in the commercial file.

Evidence before claims

Review factory and application records

See what the photographs establish, what still requires a product test, and what should be recorded in the technical agreement.

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Application review

Not sure which model fits the batch?

Share the product, batch size, container, utilities and expected production rhythm. An engineer will recommend a practical starting configuration.

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