
LPT-050S
GMP Pilot Lyophilizer
- Capacity
- 0.5 m2 shelf area
- Best fit
- Clinical, peptide and process-development batches
Pharmaceutical GMP Lyophilization
Build the lyophilizer around the product, the vial and the validation plan.
0.5-5.4 m2 shelf platforms
21 CFR Part 11-ready workflow
CIP / SIP and stoppering options
On-site commissioning support
A focused equipment range
Lyopharm Tech brings process, mechanical and compliance requirements into one pharmaceutical freeze-dryer specification. Systems support pilot and production vial lyophilization with controlled shelves, hydraulic stoppering, configurable CIP/SIP and data workflows prepared for regulated environments.
Product range

LPT-050S

LPT-100S

LPT-200S

LPT-360S
Buyer solutions
Buyer solution
Specify a compact GMP-ready pilot lyophilizer around vial count, controlled shelves, stoppering, records and qualification scope.
Primary search: 0.5 m2 pilot GMP lyophilizer
Review solution →Buyer solution
Integrate clean-in-place, steam-in-place, hydraulic stoppering, cleanroom interfaces and electronic records in a GMP lyophilizer URS.
Primary search: pharmaceutical freeze dryer CIP SIP stoppering
Review solution →Application fit
Equipment selection begins with what must be frozen, dried, documented and produced each week.
Control product temperature and mass-transfer conditions for sensitive peptide formulations.
Coordinate filling, half-stoppering, lyophilization and final stoppering as one fill-finish workflow.
Develop repeatable cycles with shelf uniformity, pressure control and documented recipes.
Use aligned control philosophy and chamber formats to reduce risk during scale-up.
Factory and application evidence

GMP configuration case
An anonymized GMP engineering case showing how vial geometry, a 13-shelf Command F stack, condenser duty and a two-working-day site scope were separated into traceable configuration decisions.
Read evidence recordCommercial 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.
Engineering view
316L product-zone surfaces, cleanable geometry and documented fabrication support regulated installation.
Fluid-controlled shelves provide repeatable temperature uniformity across freezing and drying stages.
Hydraulic stoppering, door configuration and optional barrier integration are engineered around the vial line.
PLC/SCADA architectures can support recipes, audit trail, access control and electronic batch data.
Frequently asked
Lyopharm Tech systems are manufactured by SJIA Laboratory Equipment Co., Ltd. International commercial support is provided through SJ Scientific Ltd.
Yes. Chamber format, shelves, condenser, vacuum system, controls and utilities are reviewed against the product and intended batch.
Remote support is standard. On-site installation, commissioning and operator training can be included for qualified projects.
Application review
Share the product, batch size, container, utilities and expected production rhythm. An engineer will recommend a practical starting configuration.