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Lab Semi Automatic Capsule Machine 22500 Pcs/H Herbal Capsule Maker For Clinical

Basic Properties
Place of Origin: Shanghai,China
Brand Name: TIWIN INDUSTRY
Certification: CE
Model Number: DTJ
Trading Properties
Minimum Order Quantity: 1 Set
Payment Terms: T/T
Supply Ability: 50 Sets per Month
Product Summary
Semi-automatic capsule filling machine optimized for laboratory R&D and small-batch production. Delivers 10,000-22,500 capsules per hour with minimal material waste — as little as 50g needed for fill testing. GMP-compliant stainless steel construction with quick-disassembly for validated cleaning between formulations. Ideal for pharmaceutical development, stability studies, and clinical trial material.

Product Details

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Lab semi automatic capsule machine

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semi automatic capsule machine Pcs/H

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10000pcs/h herbal capsule maker for Clinical

Model: DTJ
Capacity: 10,000-22,500 Pcs/h
Vacuum Pump: 40 M³/h
Air Compressor: 0.03m³/min, 0.7Mpa
Capsule Sizes: #000, #00, #0, #1, #2, #3, #4
Material: Food-grade Stainless Steel
Maintenance: Easy Maintenance With Modular Design
Customizationoptions: Available Based On Product And Packaging Requirements
Userinterface: Touchscreen HMI
Industry: Pharmaceutical,food,nutrition
Powersupply: 220V/380V, 50Hz/60Hz
Afrer Sale Service: 24hours In 7 Days Online Support
Product Description

Laboratory Small Batch Semi Automatic Capsule Filling Machine

Lab Small Batch Semi Auto Capsule Filler 22500 Pcs H GMP Stainless Steel for R&D Clinical Trial Production

Purpose-built for pharmaceutical R&D scientists and formulation development teams, the DTJ bridges the gap between manual hand-filling and full-scale automatic capsule production. Its 10,000-22,500 pcs/h capacity range is optimized for development batches, stability studies, and clinical trial material — providing production-representative capsule quality with the flexibility researchers need. Minimal material requirements (as little as 50g for initial testing) make it practical for expensive API development work.

Technical Specifications

Parameter DTJ
Capacity (pcs/h) 10,000-22,500
Power (kW) 2.1
Vacuum Pump (m³/h) 40
Air Compressor 0.03m³/min, 0.7Mpa
Dimensions (mm) 1,200 x 700 x 1,600
Weight (Kg) 330
Capsule Sizes #000, #00, #0, #1, #2, #3, #4
Material Food-grade stainless steel

Key Features

Laboratory-Optimized Production

  • 10,000-22,500 pcs/h capacity perfectly sized for R&D batches, stability studies, and clinical trial material
  • Precision powder filling with adjustable depth and tamping for formulation development work
  • Minimal material loss during setup — as little as 50g of formulation needed for preliminary fill testing
  • Ideal for pharmaceutical R&D labs, university research, compounding pharmacies, and nutraceutical product development

Research-Friendly Controls

  • Simple push-button semi-automatic operation — no PLC programming skills required
  • Manual control over each process step allows researchers to observe and adjust at any stage
  • Transparent guarding provides full visibility of capsule orientation, filling, and closing operations
  • Easy data recording: cycle counter, fill depth setting, and tamping pressure for lab notebook documentation

GMP & Compliance

  • Food-grade stainless steel construction meets GMP laboratory requirements
  • Quick-disassembly design for validated cleaning between formulation batches
  • CE certified — suitable for regulated development environments
  • Comprehensive documentation package for equipment qualification (IQ/OQ support available)

FAQ

How much material is needed for a test batch?
For initial fill testing, as little as 50g of powder formulation is sufficient. A full development batch with multiple fill depth settings and capsule sizes typically requires 200-500g of material to generate statistically meaningful data.
Can this machine be used for clinical trial material production?
Yes. The DTJ is widely used for Phase I and Phase II clinical trial material production where batch sizes are small (1,000-50,000 capsules). The GMP-compliant stainless steel construction and validated cleaning procedures support clinical manufacturing requirements.
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