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Inside Our Cleanroom: How ISO Class 7 Ensures Sterile Blister Packaging

زمن: June 28, 2025

Inside Our Cleanroom: How ISO Class 7 Ensures Sterile Blister Packaging


When a single dust particle can compromise an entire batch of cardiac implants, standard manufacturing won’t cut it. Our ISO Class 7 cleanroom isn’t just a “clean space”—it’s a precision ecosystem where medical-grade blister packaging achieves near-zero contamination. Here’s what happens behind the airlocked doors.


1. The Airflow Armor

Unlike typical factories, our cleanroom enforces:

  • Vertical laminar flow: 0.3-micron particles removed at 99.99% efficiency

  • Positive pressure zones: +15 Pa differential prevents external air ingress

  • Real-time particle counters: Alarms trigger at >352,000 particles/m³ (ISO threshold)

ResultSterile blister foils produced with ≤5 CFU (colony-forming units) per tray – 10× below FDA limits.


2. Gowning: Your First Line of Defense

Every technician undergoes NASA-grade protocols:

  • 30-minute air showers before entry

  • Sterile gloves changed every 45 minutes during blister sealing film handling

  • No makeup/skin exposure policies to prevent microbial shedding

Data Point: Routine swab tests show our aseptic thermoforming areas average <1 viable microorganism per 10 cm².


3. Material Decontamination Gateways

Raw materials face 3-stage purification:

  1. Gamma irradiation: For high-barrier aluminum foils used in implant packaging

  2. Non-ethanol vapor wipe-down: For PETG blister sheets (alcohol residues cause clouding)

  3. Double-bag transfer systems: With interlock pass-through chambers


4. Monitoring: Where AI Meets Asepsis

Smart systems prevent human error:

  • IoT sensors halt production if humidity exceeds 45% (prevents blister delamination)

  • Blockchain logging tracks every material batch from sterilization to sealing

  • Viable air samplers detect microbes before colonies form


Why ISO 14644-1 Class 7 Matters for You

For ophthalmic drug blister packs or surgical tool trays, this standard ensures:

  • Zero endotoxin risks: Critical for injectables

  • Consistent seal integrity: No particulates weaken blister heat seals

  • Audit-ready compliance: Full traceability for FDA/EU GMP inspections


While others claim “clean manufacturing,” we prove it with particle-per-cubic-meter accountability. Because when packaging protects lives, every micron counts.

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