Biotech R&D Heads
Series A-B startups validating lyophilization feasibility before IND. Creator gives you GMP-equivalent control architecture without GMP-scale capex.
Pilot Scale · Process Development · Tech Transfer
Creator series — 0.12 to 1.2 m² shelf area. Same control architecture as our Command GMP units, so your validated cycle scales without re-tuning. Hong Kong on-the-ground support.
Built for biotech R&D, CDMOs, and pharmaceutical process teams
Three groups buy Creator pilot systems for very different reasons. Pick yours.
Series A-B startups validating lyophilization feasibility before IND. Creator gives you GMP-equivalent control architecture without GMP-scale capex.
In-house process teams bridging lab feasibility to commercial production. Recipes export directly into Command GMP units — no protocol re-write.
Multi-client batch service providers needing flexible loading, full audit trail, and bilingual documentation for regulated customers.
Choose by shelf area. All units share the same control firmware as Command GMP.
| Model | Shelf area | Condenser temp | Typical use | |
|---|---|---|---|---|
| Creator 1S Research FD | 0.12 m² | −60 °C | Pilot batches / IND-enabling / tech transfer | View product |
| Creator 2S Research FD | 0.24 m² | −60 °C | Pilot batches / IND-enabling / tech transfer | View product |
| Creator 3S Research FD | 0.36 m² | −60 °C | Pilot batches / IND-enabling / tech transfer | View product |
| Creator 4S Research FD | 0.48 m² | −60 °C | Pilot batches / IND-enabling / tech transfer | View product |
Three representative deployments. Customer names withheld where required by NDA.
A monoclonal antibody startup at a regional Science Park ran cycle development on Creator 2S, then transferred the validated cycle directly to a Command 200F production line — no protocol changes needed.
A specialty peptide CDMO uses Creator 3S for small-batch sterile API lyophilization across 8+ client products, with full IQ/OQ/PQ documentation per batch.
A WHO-prequalified vaccine manufacturer uses Creator 4S for influenza vaccine bulk feasibility studies before scaling to Command 500F production.
For HK-based biotech and pharma R&D buyers — direct access, local invoicing, fast service.
For pilot-scale buyers, our founder is regularly in Hong Kong and available for in-person technical discussions on tech transfer strategy.
HKD quote and invoice options. Compatible with HK biotech grant and InnoHK funding documentation requirements.
In-region service across HK. No cross-border customs delay for spare parts.
Pre-installed UK-style 3-pin plug. English + 繁體中文 HMI standard. Validated documentation in both languages.
Creator matches the core specs of competitive 0.12-1.2 m² pilot units while sharing the same control architecture as our Command GMP series. That last point is the differentiator — your validated cycle scales to commercial production without re-tuning.
Yes — that is the core advantage. Recipe parameters, shelf temperature profiles, and pressure setpoints export from Creator and re-import into Command systems for controlled scale-up.
Yes. We provide batch records, controlled documentation packages, and audit-trail exports compatible with IND-enabling submissions. For full GMP qualification, our Command series is the next step.
Yes. Creator supports per-user login on the HMI; recipes, runs, and audit trail entries are tagged per user and per batch. Suitable for CDMO multi-client workflows.
Standard configurations: 8-10 weeks ex-works plus 1-2 weeks shipping. Custom configurations: add 2-4 weeks. Demo time at our HK office can be arranged for serious evaluations.
24-month warranty on chassis, refrigeration, and vacuum systems; 12 months on consumables. HK customers get on-site engineer dispatch under the warranty period. Spare parts kept in regional stock for 10 years.
A pilot freeze dryer sits between laboratory development and commercial manufacturing. The right configuration helps teams confirm cycle parameters, evaluate scale-up risk, and prepare for GMP implementation without jumping directly from bench scale to production equipment.
Compare the pilot series and GMP series together if your current objective is scale-up toward commercial manufacturing.
Tell us your formulation type, target batch size, and downstream GMP plan. Our process engineering team responds within one business day — in English or 繁體中文.