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Turnkey Biotech Cleanroom Engineering | Custom Air Filtration & Enclosures

Turnkey Biotech Cleanroom Engineering | Custom Air Filtration & Enclosures

Turnkey Biotech Cleanroom Engineering: Advanced Air Filtration & Custom Enclosures

Biomanufacturing, cell and gene therapy, and pharmaceutical processing require rigid environmental stability and stringent contamination control. Delivering a fully compliant, cGMP-grade environment demands a seamless integration of structural enclosures, HVAC precision, and high-performance air filtration. Farclean provides comprehensive, end-to-end turnkey cleanroom engineering solutions designed to meet ISO 14644-1 and EU GMP Grade A–D standards from concept to final validation.


1. Integrated Modular Cleanroom Architecture

A successful biotechnology cleanroom starts with robust, non-shedding, and easily decontaminated structural architecture. Farclean’s modular wall and ceiling enclosure systems are engineered specifically for demanding biopharmaceutical applications:

  • High-Performance Panel Cores: Manufactured with rockwool, PIR, or aluminum honeycomb cores to offer superior thermal insulation, sound dampening, and fire resistance.
  • Smooth, Flush-Mounted Design: All wall panel joints, walkaway ceiling grids, view windows, and integrated cleanroom doors feature smooth, flush transitions to prevent particle accumulation and facilitate thorough cleaning.
  • VHP Decontamination Compatibility: Wall surfaces are finished with specialized HPL, stainless steel, or anti-microbial powder coatings capable of withstanding frequent Vaporized Hydrogen Peroxide (VHP) sterilization cycles.
  • Pressure Cascade Airlocks: Engineered airlock systems (bubble, sink, and cascade options) with interlocked door mechanisms maintain stable differential pressure barriers across ISO Class 5 to 8 cleanrooms.

2. Precision Custom Air Filtration & Environmental Control

Air purity is the core component of biological containment and product protection. Farclean customizes air handling units (AHU) and filtration networks to deliver precise, contamination-free air streams:

  • Terminal HEPA & ULPA Modules: Equipped with H14 HEPA (≥99.995% efficiency) or U15–U17 ULPA filters paired with energy-efficient ECM fan filter units (FFU) for consistent laminar airflow.
  • Strict Atmospheric Control: Advanced HVAC configurations ensure tight temperature control (±0.5°C) and relative humidity regulation for low-dewpoint bioprocessing areas.
  • Containment & Safe-Change Systems: High-containment exhaust systems featuring Bag-In/Bag-Out (BIBO) housings safeguard operators and the outside environment when handling hazardous biological materials or active compounds.

3. Localized Enclosures & Containment Workstations

To optimize operational efficiency, Farclean integrates localized micro-environments and material transfer systems directly into facility designs:

  • Aseptic Barrier Isolators: ISO Class 5 / Grade A barrier isolators designed for sterile filling, compounding, and quality control.
  • Sampling & Dispensing Booths: Custom downflow booths and laminar flow workstations with continuous particulate monitoring.
  • Dynamic Pass Boxes & Air Showers: Interlocked transfer chambers with optional HEPA recirculation and VHP integration to eliminate cross-contamination during material entry.

Key Technical Specifications

Parameter Specification Standard
Cleanroom Classification ISO Class 3 to ISO Class 8 / EU GMP Grade A, B, C, D
Compliance Frameworks US FDA cGMP, EU Annex 1, ISO 14644, USP <797>/<800>
Filtration Rating HEPA H14 (≥99.995% @ MPPS) / ULPA U15–U17
Enclosure Finishes Flush-fit modular panels; Powder-coated galvanized steel / HPL / SS 304/316L
Sterilization Compatibility Vaporized Hydrogen Peroxide (VHP), Peracetic Acid, Quaternary Ammonium

Target Industry Applications

  • Biopharmaceuticals: Bioreactor processing rooms, downstream purification suites, and fill-finish suites.
  • Cell & Gene Therapy (CGT): High-containment suites operating under positive or negative pressure cascades for viral vector production.
  • Medical Device Manufacturing: Sterile assembly and packaging environments compliant with ISO 13485.
  • Compounding Pharmacies: Fully compliant USP <797> sterile compounding and USP <800> hazardous drug processing enclosures.
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