logo
Welcome to Shanghai TIWIN Industry Co., Ltd.
+8618621833870
Home / Products / Tablet Press Machine / TEU-H65 Automatic GMP Double Layer Pharmaceutical Tablet Press Machine 65 Stations B Tooling 280800 Pcs/Hr CE
Quality TEU-H65 Automatic GMP Double Layer Pharmaceutical Tablet Press Machine 65 Stations B Tooling 280800 Pcs/Hr CE factory
Quality TEU-H65 Automatic GMP Double Layer Pharmaceutical Tablet Press Machine 65 Stations B Tooling 280800 Pcs/Hr CE factory

TEU-H65 Automatic GMP Double Layer Pharmaceutical Tablet Press Machine 65 Stations B Tooling 280800 Pcs/Hr CE

Basic Properties
Place of Origin: Shanghai,China
Brand Name: TIWIN INDUSTRY
Certification: CE
Model Number: TEU-H65
Trading Properties
Minimum Order Quantity: 1 Set
Payment Terms: T/T
Supply Ability: 10 Sets per Month
Tags

rotary tablet press

pill tablet press

pharmaceutical tablet press
Product Summary
Automatic GMP double layer pharmaceutical tablet press TEU-H65 with 65 B-type punch stations, 280,800 tablets/hour, 100kN, cGMP sanitary design, dual force feeders, AWC, 21 CFR Part 11 PLC, and full IQ/OQ/PQ documentation.

Product Details

Highlight:

GMP Double Layer Tablet Compression

,

cGMP Bi-Layer Pharmaceutical Tablet Press

,

FDA 21 CFR Part 11 Press
No. Of Punch Stations: 65
Punch Type: B
Main Compression (KN): 100
Capacity (Pcs/H): 280,800
Max. Tablet Diameter (Mm): 16
Max. Filling Depth (Mm): 16
Control System: German PLC With 21 CFR Part 11
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
Automatic GMP Double Layer Pharmaceutical Tablet Press Machine TEU-H65
The TEU-H65 is a fully automatic rotary tablet press purpose-built for double-layer (bi-layer) pharmaceutical tablet production in strictly regulated cGMP manufacturing environments. Equipped with 65 B-type punch stations producing 280,800 tablets per hour, this machine delivers the optimal balance of high productivity and pharmaceutical-grade precision for medium to large-scale solid dosage operations. Every aspect of its design from the sealed compression cabin to the validated control system is engineered for full regulatory compliance.
This double-layer tablet press features independent dual force-feeding systems with vacuum dust extraction, real-time automatic weight control (AWC) with individual layer sampling, 100kN main compression, and a fully enclosed sanitary design with quick-disassembly product contact parts. The German PLC with 21 CFR Part 11 compliant controls provides multi-level security, electronic batch records, and comprehensive audit trails required by FDA, EMA, and international regulatory agencies.
Key Features
  • Full cGMP Compliance Design: Sealed compression cabin, sanitary SUS304/SUS316 contact surfaces, HEPA-filtered dust extraction, and fully documented IQ/OQ/PQ validation package.
  • Double-Layer Tablet Technology: Two independent filling and pre-compression stations produce perfectly bonded bi-layer tablets with clearly defined layer separation and zero cross-contamination risk.
  • 21 CFR Part 11 Control System: German PLC with electronic signatures, multi-level password protection, secure data logging, and full audit trail capability for regulatory inspections.
  • Precision Weight Control: Real-time AWC system with independent first-layer sampling capability maintains both layers within pharmacopoeia weight tolerances throughout production runs.
  • Rapid Sanitary Changeover: All product contact parts feature tool-free quick-disassembly for efficient cleaning validation between products and formulations.
  • Single-Layer Flexibility: Easily switchable to single-layer mode via HMI for maximum equipment utilization across your product portfolio.
Technical Specifications
Parameter TEU-H65
Number of punches 65
Punch type B
Punch shaft diameter (mm) 19
Die diameter (mm) 30.16
Die height (mm) 22.22
Main pressure (kN) 100
Pre-pressure (kN) 100
Turret speed (rpm) 72
Capacity (pcs/h) 280,800
Max. tablet diameter (mm) 16
Max. irregular-shaped length (mm) 19
Max. tablet thickness (mm) 8.5
Max. filling depth (mm) 16
Voltage 380V/3P 50Hz (customizable)
Main motor power 11 kW
Pitch circle diameter 720 mm
Machine dimension 1,300 * 1,300 * 2,125 mm
Operation cabinet dimension 704 * 600 * 1,300 mm
Net weight 5,000 kg
Frequently Asked Questions
Q1: What makes this machine specifically GMP-compliant?
A: The TEU-H65 is designed from the ground up for cGMP facilities: fully enclosed sealed compression cabin with HEPA extraction, SUS304/SUS316 sanitary product contact surfaces with surface finish certification, tool-free quick-disassembly for validated cleaning, complete IQ/OQ/PQ documentation, and 21 CFR Part 11 compliant controls with full audit trail capability.
Q2: Can this machine be used in an EU GMP Annex 1 or FDA sterile manufacturing facility?
A: The TEU-H65 is designed for solid dosage (non-sterile) manufacturing. For facilities requiring containment down to OEB 4-5 (highly potent compounds), we offer optional isolation packages including negative pressure cabin, continuous liner systems, and wash-in-place (WIP) capabilities. Please contact us for custom containment configurations.
Q3: How is cleaning validation supported?
A: All product contact parts disassemble without tools in under 15 minutes. The design eliminates dead spaces and crevices. We provide surface finish certification (Ra ≤ 0.8μm standard, Ra ≤ 0.4μm optional), material certifications, and full cleaning validation support documentation including recommended cleaning agents and procedures.
Q4: What documentation comes with the machine for regulatory filing?
A: Standard documentation includes: CE declaration, material certifications (SUS304/SUS316), surface finish reports, IQ/OQ/PQ protocol templates, Factory Acceptance Test (FAT) report, Site Acceptance Test (SAT) protocol, control system validation package, and 21 CFR Part 11 compliance documentation.
Q5: How long does a product changeover take?
A: A complete deep cleaning and formulation changeover typically takes 1.5-2.5 hours depending on operator experience. Recipe parameters for up to 50 products are stored in the PLC and recalled via touchscreen in seconds.
Q6: Can the TEU-H65 handle modified-release and combination bi-layer tablets?
A: Yes. This is one of its primary applications. The independent compression control for each layer allows precise engineering of immediate-release and sustained-release profiles within a single bi-layer tablet. It is widely used for combination tablets  requiring controlled release kinetics.
Q7: Do you provide on-site validation support?
A: Yes. Our engineering team provides on-site installation, commissioning, IQ/OQ execution, and operator training. We also offer periodic requalification services and calibration support for the compression force sensors and control instrumentation.
Q8: What are the payment and delivery terms?
A: Standard payment terms are T/T with 30-45 working days delivery after deposit confirmation. Express delivery options and installation scheduling are available to align with your facility qualification timelines.

Miss. Toi Foo

Related Products

Send An Inquiry