Equipment

GMP Capsule Ancillary Equipment — Dedusters, Capsule Polishers Washers & More

Hard Capsule Post-Processing, Softgel Washing & Drying, Quality Control Solutions.

GMP-Validated Cleaning, Moisture-Controlled Processing, Integrated Quality Control.

LOCUS GROUP supplies GMP-compliant capsule dedusters and polishers — essential post-encapsulation equipment for:

  • Removing residual powder from capsule surfaces

  • Eliminating static charge

  • Achieving pharma-grade visual quality

  • Ensuring compliance with USP <1061> and EU GMP Annex 15


LOCUS ROBOTICS delivers validated auxiliary equipment for complete hard and soft gelatin capsule production lines. We engineer integrated solutions from encapsulation to final inspection — ensuring GMP compliance at every stage.

Hard Gelatin Capsule Systems

Equipment Function GMP Features
Capsule Dedusters Remove residual powder particles HEPA filtration (99.97% @ 0.3µm)
Polishing Drums Enhance surface finish Anti-static brushes
Visual Inspection Backlit panels for defect detection ISO 15378-compliant lighting
Calibration Units Verify capsule thickness/density Automated rejection systems
Laser Markers Product identification 21 CFR Part 11 data logging

Softgel Capsule Systems

Equipment Function Specialized Features
Ethanol Drum Washers Remove surface residues Explosion-proof construction
Humidity-Controlled Dryers Moisture stabilization (20-30% RH) CIP/SIP capability
Rotary Die Test Stations Validate die engraving quality Precision micrometer adjustment
Gelatin Reactors Prepare encapsulation mass Jacketed heating/cooling
Ethanol Storage Tanks Solvent containment Nitrogen blanketin

Equipment Specifications

Model Type Capacity Key Features
Benchtop Polisher 500-2,000 caps/hr • Compact footprint (40×40cm)
• Food-grade PVC drum
• Manual loading/unloading
Industrial Deduster 20K-100K caps/hr • CIP/SIP capability
• HEPA filtration (99.97% @ 0.3µm)
• Humidity control (30-50% RH)
Pharma-Grade System 50K-200K caps/hr • Integrated metal detection
• Data logging (21 CFR Part 11)
• Viable particle monitoring

Technical Process

Technical Process Flow

GMP Compliance Framework

  • Material Contact: AISI 316L stainless steel surfaces

  • Validation Packages: IQ/OQ/PQ protocols for:

    • FDA 21 CFR Part 211

    • EU Annex 1

    • WHO TRS 1033

  • Critical Parameters:

    • Airflow: 0.45 m/s ±10% (dedusters)

    • RH Control: ±2% tolerance (dryers)

    • Temperature: ±0.5°C (gelatin reactors)

Capsules enter rotating brush chamber → Static-free bristles remove particles → HEPA-filtered vacuum extracts residue → Cleaned capsules discharge via vibratory chute

Critical GMP Features

  • Material Contact: AISI 316L stainless steel surfaces

  • Cleanability: Ra <0.8 µm surface finish

  • Documentation: IQ/OQ protocols included

  • Environmental Control:

    • Humidity regulation (±5% RH)

    • Temperature monitoring (15-25°C)

    • Laminar airflow (ISO Class 7 equivalent)

Regional Adaptations

Market Special Configuration
Southeast Asia Tropical package: Dehumidifier + corrosion-resistant coating
Africa Voltage stabilizer (110-480V input)
Middle East Arabic HMI interface + dust-proof electronics
Market Equipment Modification
Southeast Asia Tropical package: Dehumidifiers + corrosion-resistant coatings
Africa Voltage stabilizer (90-480V input)
Middle East ATEX-certified ethanol handling
Latin America Spanish/Portuguese HMI interfaces

Integration Options

Technical Comparison

Parameter LOCUS

LCPDC-10

Industry Average
Throughput 80K caps/hr 50K caps/hr
Particle Removal 99.2% @ >5µm 95.1%
Power Consumption 1.2 kW 2.5 kW
CIP Time 18 minutes 45 minutes

Integration Capabilities

+ Seamless connection to encapsulation machines
+ Unified control system (OPC-UA protocol)
+ Automated material transfer between stations
- No manual handling between processes

Technical Comparison

Parameter LOCUS Systems Industry Standard
Dedusting Efficiency 99.2% @ >5µm particles 96.5%
Drying Time 20-40 min (softgels) 60-90 min
Changeover Tool-free <15 min 45-60 min
Power Consumption 30% lower Baseline

Precision Engineering:

Our anti-static brush technology reduces particle adhesion by 66% — critical for hygroscopic APIs in high-humidity environments.

Our Teflon-coated polishing drums eliminate micro-scratches — critical for hygroscopic formulations in high-humidity environments.

Regulatory Excellence:

Full electronic batch records comply with EU Annex 11 — including environmental monitoring data for RH, particles, and airflow.

Full audit trail documentation meets FDA 21 CFR Part 11 requirements — including particle count logs and humidity cycle records.

Competitive Advantages

+ 40% faster dust removal vs. industry average  
+ Patented anti-static brushes (RU Patent #2023142117)  
+ Integrated weight loss monitoring (<0.1% product loss)  
- Zero compressed air requirement  

Efficiency Gains:

Integrated ethanol recovery systems reduce solvent consumption by 55% versus conventional softgel washing lines.

Process 100,000 capsules/hour with <0.3% damage rate — 5X faster than manual wiping with 90% labor reduction.

Hard Gelatin Capsule Dedusting and Polishing Systems.

GMP capsule deduster industrial model.

Pharma polishing drum 316L stainless.

GMP capsule deduster HEPA filtration.

Softgel ethanol washing drum 316L.

Achieve Pharma-Grade Perfection!

Complete Your Capsule Production Line!

Ready to Eliminate Production Bottlenecks?

Need Pharm Production Automation?

✅ GMP Compliance Guarantee

✅ 24/7 Multilingual Support

✅ 24-month performance guarantee

✅ Local technicians in 18 countries

Start small, get a free production layout designed for your growth trajectory. Scale smarter with engineering support!

Free line configuration for your products, throughput validation testing!

Contact Specialists for GMP:

📞 Phone: +7 927 056-19-99
Voltage customization available (110V-220V-380V-480V) — trusted by Pharm manufacturers in 16+ countries. Serving manufacturers in 12+ countries across Africa, SE Asia & MENA.
Support: EN/RU/AR/ES — On-site commissioning available globally. Includes 24/7 remote monitoring and validation support (IQ/OQ/PQ).
Multi-language HMIs, regional certifications included (International calls routed to English-speaking engineers).

Compliance Roadmap:

  • CE, EAC, ISO 9001 certifications.

  • GMP-ready: 316L SS contact parts, CIP/SIP capabilities.