Equipment

Monobloc Systems for Tablet and Capsule Packaging

GMP-Compliant Integrated Packaging for Solid Dosage Forms.

Precision-Engineered Solid Dosage Packaging
Integrated rotary systems combining counting, bottle filling, cotton insertion, and induction sealing in ISO Class 8 environments — designed for GMP compliance of hard/soft gelatin capsules and coated tablets.

Precision Engineered for Pharma Integrity
Integrated counting, filling, cotton insertion, and sealing in ISO Class 8 equivalent environments — designed for uncompromised product protection of solid dosage forms.

Critical Components:

Technical Specifications

Pharmaceutical-Grade Performance

Parameter Standard Specs Premium Options
Throughput 80-150 BPM 300 BPM (high-speed)
Counting Accuracy 100% ±0 tablets Vision-verified
Container Range 20-100mm jars Vials to 1L bottles
Dosage Forms Tablets • Hard Capsules Softgels • Lozenges
Environmental Control ISO Class 8 equivalent Isolated RABS option
Compliance GMP • 21 CFR Part 11 EU Annex 1

Core Capabilities:

Technical Specifications

Pharmaceutical-Grade Performance

Parameter Standard Range Premium Options
Throughput 80-150 BPM 300 BPM (servo-driven)
Counting Accuracy 100% ±0 tablets Vision verification
Dosage Forms Hard/Soft Gel Caps • Coated Tabs Lozenges • Gummies
Container Compatibility Glass/Plastic Bottles (20-200mm) Vials • Jars
Environmental Control ISO Class 8 Equivalent Isolated RABS Option

Dosing Technology Comparison

Precision Counting Mechanisms

System Best For Accuracy Speed
Rotary Disc Counter Standard tablets/capsules 100% ±0 200 units/min
Vibratory Feeder Irregular shapes/sizes 99.98% 150 units/min
Multi-Lane Counter High-volume production 100% ±0 500 units/min
Vision-Verified Coated/printed dosage forms 100% defect-free Custom

Pharmaceutical Validation

Critical Compliance Features

  • Material Construction: AISI 316L SS contact surfaces

  • Cleanability: CIP/SIP capability, radiused corners

  • Data Integrity: Electronic batch records with audit trails

  • Change Control: Documented SAT/FAT protocols

  • Environmental: HEPA-filtered air showers

GMP-Compliant Workflow

Seamless 8-Stage Processing

  1. Bottle Unscrambling: Orientation verification

  2. Precise Counting: Vibration-free disc technology

  3. Gentle Transfer: Low-friction PU channels

  4. Cotton Insertion: Anti-static placement (optional)

  5. Induction Sealing: 1-5kW foil sealing

  6. Torque Capping: 1-20Nm servo application

  7. Quality Control: Checkweighing ±0.5g

  8. Downstream Integration: Labeling • Cartoning


Cleanroom Integration

Critical Area Protection

  • HEPA-Filtered Enclosures: ISO 14644-1 Class 8

  • Material Pass-Throughs: Rapid transfer ports

  • GMP-Grade Surfaces: 316L SS • Pharma plastics

  • Contamination Control: Negative pressure zones


Specialized Applications

Optimized Dosage Form Handling

Dosage Form Special Features
Enteric-Coated Tabs Anti-abrasion channels
Softgel Capsules Temperature-controlled transfer
Hygroscopic Forms <20% RH nitrogen-purged environment
Omega-3 Softgels Cold-chain compatible components

Optional Upgrades

Enhanced Compliance & Efficiency

  • Isolation Technology: RABS or isolator integration

  • Track & Trace: Serialization modules (DSCSA/FMD compliant)

  • Vision Inspection: 100% defect detection

  • Nitrogen Flushing: <50ppm O₂ residual control

Upstream Integration

Complete Production Line Solutions


Competitive Advantages

Why Pharmaceutical Manufacturers Choose Locus
✅ Zero Product Damage: <0.1% friability rate
✅ Rapid Changeovers: <10 mins between formats
✅ Regulatory Ready: IQ/OQ/PQ validation packages, Full validation packages
✅ Scale Flexibility: Modular capacity expansion


Compliance Framework

Global Regulatory Alignment

Standard Implementation
GMP (WHO/EU/US) Full documentation packages
21 CFR Part 11 Audit trails • E-signatures
EU Annex 1 Isolated critical zones
PIC/S Cross-border compliance

Global Compliance Support

Schedule a validation consultation:

📞 Phone: +7 927 056-19-99
FAT/SAT protocols included • Multi-language documentation • Local compliance experts • EU Annex 1 • PIC/S GMP • WHO compliance frameworks supported
(International calls routed to English-speaking engineers).