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ENGINEERING DOSSIER REF: BC-CASE-GMP2025 WHO-GMP & PIC/S VALIDATED LOCATION: SOUTHEAST ASIA

Pharma Cleanroom Suite: 1,650 m² Sterile Formulation & Filling

Engineered to WHO-GMP and PIC/S standards: Grade A laminar filling hood, Grade B background clean suite, liquid gel-seal HEPA diffusers, self-purifying dynamic pass boxes, and full DQ/IQ/OQ validation handover.

Project Scope & Regulatory Challenges

A regional pharmaceutical producer required a brand-new sterile liquid formulation and aseptic filling wing covering 1,650 m². The architectural and HVAC envelope had to satisfy stringent WHO-GMP guidelines with four environmental tiers: Grade D personnel gowning and washing airlocks, Grade C raw formulation preparation, Grade B cleanroom suite, and Grade A unidirectional laminar airflow over the open sterile ampoule filling conveyor.

Critical Compliance Gaps Addressed: The buyer required absolute zero bypass leakage on all ceiling terminal diffusers, seamless antimicrobial flush panel joints resistant to continuous vaporized hydrogen peroxide (VHP) decontamination, and calibrated on-site particle counter test logs to secure national Ministry of Health drug manufacturing licensing.

BESTCLEAN Integrated Engineering Package: BESTCLEAN provided complete cleanroom architectural envelope manufacturing (50mm aluminum honeycomb panels, flush coved SUS304 frames), proprietary knife-edge gel-seal HEPA terminal filter housings, laminar flow dynamic pass boxes with differential pressure gauges and DOP aerosol test ports, and dispatch of commissioning validation engineers with calibrated Met One laser particle counters.

TOTAL CLEAN SUITE AREA
1,650 m²
AIRBORNE CLASSIFICATION
Grade A, B, C, D
CASCADE DIFFERENTIAL
+15 Pa / +30 Pa
VALIDATION HANDOVER
DQ / IQ / OQ Approved

Authentic Project & Qualification Records (Pharma Clean Suite)

Photographs from architectural BIM cutaway modeling, jobsite clean suite installation, and particle validation:

Pharmaceutical Equipment & Component Schedule (BOM)

System / Category Delivered Specification & Equipment Model Quantity Regulatory & Validation Protocol
Wall & Ceiling Panels 50mm Aluminum Honeycomb Sandwich Panels (0.6mm PPGI skins, non-combustible) 2,600 m² VHP resistant, flush R50 coved aluminum transition profiles
Gel-Seal HEPA Units BJ-GST Liquid seal terminal diffusers + H14 PTFE mini-pleat filters (99.995% @ 0.3µm) 112 sets DOP aerosol challenge injection port + upstream sampling port
Dynamic Pass Boxes BJ-PB800-D SUS304 Dynamic Laminar Flow Pass Box with Magnehelic gauge & UV 8 units Class 100 internal cleanliness, electronic interlock, HEPA filtered
Airtight Pharma Doors SUS304 Flush Cleanroom Doors with flush double-pane viewing windows 36 sets Concealed automatic acoustic drop sweeps, German dormakaba hardware
AHU Purification HVAC Double-skin hygienic AHUs with inverter EC plug fans (22,000 m³/h capacity) 4 systems DIN 1946-4 hygienic design, steam humidifiers, chilled water cooling coils
Hygiene Scrub Stations SUS304 3-station surgical sensor handwashing sink with integral backsplashes 4 sets Touchless infrared sensors, thermostatic mixing, medical scrub standard

GMP Handover: Full DQ / IQ / OQ Qualification Package

PHARMACEUTICAL COMPLIANCE DOSSIER

Audit-Ready Documentation Provided with Every Delivered Clean Suite

BESTCLEAN delivers comprehensive FAT/SAT and qualification protocols so pharmaceutical clients pass GMP inspections on the first attempt without regulatory delay:

  • Design Qualification (DQ): Complete architectural zoning drawings, differential pressure hierarchy mapping (+30/+20/+10 Pa), airflow balance calculations, and material traceability certificates (SUS304 mill test, PPGI food/pharma grade coatings).
  • Installation Qualification (IQ): As-built CAD blueprints, duct pressure leak test logs, HEPA filter factory DOP scan certificates, instrument calibration certificates (traceable to NIST/CNAS).
  • Operational Qualification (OQ): On-site airborne particle count testing at rest (ISO 14644-1), filter face air velocity uniformity tests (0.45 m/s ±20%), room recovery time tests (< 15 minutes), and differential pressure cascade verification.
  • Performance Qualification (PQ) Support: Background bioburden baseline sampling protocols, continuous particulate monitoring system (CPMS) sensor layout recommendations, and HVAC damper rebalancing.

Planning a Pharmaceutical GMP Cleanroom or Sterile Suite?

Consult with our senior cleanroom engineers for HVAC cascade design, equipment selection, and full qualification support.

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