AAF Pharmaceutical Filters

Người đăng: VIETPHAT | 01/04/2025

AAF Pharmaceutical Filters: High-Efficiency Air Filtration for Critical Pharmaceutical Environments

In pharmaceutical manufacturing, air purity is not just important—it’s mandatory. From cleanrooms to sterile production lines, every cubic meter of air must be carefully controlled to meet strict regulatory standards and prevent contamination. That’s why pharmaceutical manufacturers worldwide rely on AAF Pharmaceutical Filters—advanced air filtration solutions that provide unmatched performance, compliance, and safety in the most demanding environments.

Backed by over a century of filtration expertise, AAF International offers a full suite of filters tailored specifically for the GMP-compliant pharmaceutical industry, ensuring optimal product integrity and cleanroom compliance.

What Are AAF Pharmaceutical Filters?

AAF Pharmaceutical Filters are a specialized range of high-efficiency air filters designed to remove airborne particles, microbes, and molecular contaminants from air supply systems in pharmaceutical production facilities, laboratories, and cleanrooms. These filters are engineered to meet stringent standards such as:

✅ EU GMP (Grade A/B/C/D)
✅ FDA cGMP
✅ ISO 14644 Cleanroom Standards
✅ WHO Guidelines for Sterile Manufacturing

From HEPA and ULPA filters for clean zones to gas-phase filters for odor and VOC control, AAF provides a full clean air solution for the pharmaceutical industry.

Key Features of AAF Pharmaceutical Filters

✅ HEPA/ULPA Filtration: ≥99.97% to ≥99.999995% efficiency for particles as small as 0.12 microns
✅ Molecular Filtration: Removes airborne molecular contaminants (AMCs), VOCs, and odors
✅ GMP-Grade Materials: Cleanroom-compatible construction, corrosion-resistant frames, low-outgassing materials
✅ Leak-Free Sealing: Gel seal, knife-edge, or gasket options to ensure zero bypass
✅ Certified Performance: Each filter is individually tested per EN 1822, ISO 29463, or IEST-RP-CC001
✅ Compliance Documentation: Full traceability, batch tracking, and test certificates provided

Why Use AAF Filters in Pharmaceutical Manufacturing?

1. Protect Product Purity

Airborne particles, bacteria, and VOCs can compromise the safety and efficacy of pharmaceutical products. AAF filters remove these contaminants at the source—ensuring clean air for clean production.

2. Meet Regulatory Compliance

With certifications for HEPA integrity, air cleanliness, and microbial control, AAF filters support GMP audits, FDA inspections, and ISO 14644 validations with confidence.

3. Support Cleanroom Classification

AAF filters help maintain ISO Classes 5 to 8 cleanroom environments for different pharmaceutical zones (sterile filling, weighing, compounding, etc.).

4. Reduce Downtime & Maintenance

High dust-holding capacity and robust construction mean longer service life, less frequent replacements, and stable airflow performance.

Common Pharmaceutical Applications

Area	Recommended Filters
💉 Sterile Manufacturing	HEPA/ULPA terminal filters, ceiling modules (Grade A/B)
⚗️ Compounding & Weighing Areas	HEPA filters, BioCel® V, DriPak® 2000
💊 Tablet & Capsule Production	MERV 14–16 rigid filters, pre-filters, molecular filters
🧪 QC Labs & R&D Centers	HEPA filters, activated carbon panels
🏥 Cleanroom HVAC Systems	Pre-filter + fine filter + HEPA final filter setup
🚮 Waste Handling Zones	SAAF™ odor and chemical gas filters

Types of AAF Pharmaceutical Filters

🔹 AstroCel® II HEPA & ULPA Filters

H13–U17 efficiency
Individually scan-tested and certified
Ideal for cleanrooms, isolators, and biosafety cabinets

🔹 BioCel® V Rigid Filters

MERV 14–16 (ISO ePM1 85%)
Pre-final filter for clean zones and HVAC AHUs

🔹 DriPak® 2000

Extended surface pocket filter
Excellent dust-holding capacity and low resistance
Used as intermediate or final filters in Grade C/D areas

🔹 PerfectPleat® & Pre-Filters

MERV 8–13
Protect higher-efficiency filters and improve system efficiency

🔹 SAAF™ Gas Phase Filters

Activated carbon or impregnated alumina
Controls VOCs, solvents, formaldehyde, and cleanroom odors

Technical Specifications Overview

Parameter	Typical Values
HEPA/ULPA Efficiency	≥99.97% to ≥99.999995% @ 0.3 to 0.12 microns
Filter Ratings	H13–U17 (EN 1822), MERV 14–16 (ASHRAE 52.2)
Filter Media	Glass microfiber, synthetic, activated carbon
Frame Materials	Aluminum, stainless steel, galvanized steel
Seal Types	Gel seal, knife-edge, gasket
Operating Temp Range	Up to 70°C – 120°C depending on model
Humidity Resistance	100% RH (non-condensing)
Testing Standards	EN 1822, ISO 29463, IEST-RP-CC001

Why Buy AAF Pharmaceutical Filters from VIETPHAT?

As an authorized distributor of AAF International in Vietnam, CÔNG TY CỔ PHẦN KỸ THUẬT VIỆT PHÁT offers:

🧠 Technical support for GMP cleanroom HVAC design and filter selection
📦 Ready stock of certified filters in multiple sizes and ratings
🧪 On-site filter testing (PAO/DOP leak tests, particle counts, ISO 14644 validation)
🔧 Installation guidance and maintenance training
📋 Compliance documentation (COC, COA, batch records, filter maps)

📞 Hotline: 0971 344 344
📧 Email: sales@vietphat.com
🌐 Website: www.vietphat.com

Conclusion

With increasingly strict air quality standards and the critical need for contamination control, pharmaceutical manufacturers must rely on filtration solutions that deliver more than just clean air—they must deliver precision, consistency, and compliance. That’s exactly what AAF Pharmaceutical Filters offer: world-class protection for your products, processes, and people.

✅ Certified Clean Air. Proven Performance. Pharmaceutical Peace of Mind. Trust AAF.