
LPT-050S
GMP Pilot Lyophilizer
- Capacity
- 0.5 m2 shelf area
- Best fit
- Clinical, peptide and process-development batches
Pharmaceutical GMP Lyophilization
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
Open any model for its manufacturing reference and published engineering data.

LPT-050S

LPT-100S

LPT-200S

LPT-360S

LPT-500S
Model comparison
Published values are a planning reference. Confirm the product or formulation, loading format, endpoint, utilities and complete cycle before purchase.
| Model | Reference capacity | Loading format | Condenser | Best fit |
|---|---|---|---|---|
| LPT-050S | 0.5 m2 shelf area | Pilot vial loading | <= -85 C | Clinical, peptide and process-development batches |
| LPT-100S | 1.0 m2 shelf area | Pilot / small production | <= -85 C | Sterile injectables and biotech production |
| LPT-200S | 2.16 m2 shelf area | Production vial loading | <= -85 C | Commercial peptide and injectable lines |
| LPT-360S | 3.6 m2 shelf area | Configurable shelf count | Matched production condenser | Medium-scale commercial fill-finish |
| LPT-500S | 5.4 m2 shelf area | Large production loading | <= -85 C | High-capacity regulated production |
Commercial confidence
No invented stock, delivery date or universal performance promise. The commercial file connects the machine to an approved technical basis.
Lyopharm Tech / SJIA manufacturing platform remains visible from quotation and technical agreement through manuals, spare parts and service.
Capacity, utilities, interfaces, options and acceptance conditions are recorded before manufacturing release.
The agreed FAT scope can cover dimensions, controls, alarms, refrigeration, vacuum and documentation checks.
Packing, shipping terms, lead time, installation access and site responsibilities are confirmed in the quotation.
Remote support is standard; qualified projects can include on-site installation, commissioning and operator training.
Warranty scope, exclusions, service route, consumables and recommended spare parts are stated in the commercial file.
Evidence before claims
See what the photographs establish, what still requires a product test, and what should be recorded in the technical agreement.
Browse 1 casesApplication review
Share the product, batch size, container, utilities and expected production rhythm. An engineer will recommend a practical starting configuration.