Description

Sterile and Precise Filling for Pharmaceutical Preparations

Engineered for Pharmaceutical Excellence.

In GMP-regulated pharmaceutical environments, precision, sterility, and validation are paramount. The LFP-10 is designed to meet these needs with a contamination-free pumping principle and independent channel control. This system is perfectly suited for R&D laboratories, pilot plants, and small-to-medium batch production of critical liquid pharmaceuticals.

Technical Highlights and Key Features

• Two Independent Pump Heads: Allows for simultaneous operation with different fill volumes or products, providing flexibility and doubling productivity compared to single-head units.

• High-Precision Dosing: Peristaltic technology is known for its high volumetric accuracy. Similar systems achieve flow accuracies of 0.2% or better, ensuring each container receives the exact same dose, which is critical for pharmaceutical efficacy and safety.

• Sterile, Single-Use Fluid Path: The product only contacts the disposable tubing. This closed system prevents cross-contamination between batches, eliminates cleaning validation for the fluid path, and is ideal for aseptic processing.

• User-Friendly Control with Advanced Features: Features a programmable controller (potentially with a touchscreen) for setting fill volumes and storing recipes. Key features for pharmaceuticals include an anti-drip function to ensure dispense accuracy and maintain a clean work area, and reversible operation to clear lines or recover excess product.

• GMP-Friendly Construction: The external housing is likely made of robust, cleanable materials such as ABS plastic or stainless steel, suitable for controlled environments.

Industries and Applications

The LFP-10 is specialized for sectors requiring the highest levels of purity and accuracy:

• Pharmaceuticals & Biologics: Aseptic filling of vaccines, injectable drugs, IV fluids, and diagnostic reagents.

• Medical Devices: Dispensing sterile solutions for medical device kits.

• Cosmetics: Packaging of sterile, preservative-free serums and topical solutions.

Why Choose This System?

• Regulatory Compliance: The design supports compliance with stringent FDA, EMA, and other international GMP standards for aseptic processing.

• Reduced Contamination Risk: The closed-system design is a key engineering control to minimize microbial and particulate contamination.

• Operational Efficiency: Dual-head filling increases output, while the single-use tubing eliminates complex Clean-in-Place (CIP) systems for the fluid path, reducing changeover time.

📜 Schedule virtual airflow visualization test.

💡 Mention your: Target market (EU/US/Global South), Active ingredient, Required throughput.

🔬 Schedule virtual factory acceptance test with our engineers.

🏷️ Request Compliance Audit: Free gap analysis with throughput simulation.

🔍Ready to Eliminate Production Bottlenecks?

💎Need Industrial Production Automation?

📥Free line configuration for your products, throughput validation testing!