Taizhou, China – April 2025 – Besin Environmental Protection Technology (Taizhou) Co., Ltd., a pioneer in bio-pharmaceutical cleanroom air purification, has introduced its revolutionary ultra-micro electrostatic filter technology, offering a superior alternative to traditional medium-efficiency filters in pharmaceutical cleanroom applications.
With the rigorous enforcement of GMP (Good Manufacturing Practice) and ISO 14644 standards, pharmaceutical cleanrooms demand higher air cleanliness than ever before. Conventional medium-efficiency filters, however, suffer from high consumable costs, inefficient dust retention, safety concerns, and labor-intensive maintenance—posing significant challeng
es for the industry.
Besin’s proprietary ultra-micro electrostatic air filter employs an interlaced electrode membrane design, generating a high-intensity electric field that ensures efficient air purification and instant microbial disinfection, surpassing the limitations of traditional filtration methods.
✔ Superior Dust Retention – 325 mg/(m³/h) dust-holding capacity (9× higher than national standards), extending maintenance intervals to 1 year.
✔ Washable & Reusable – Withstands 100+ wash cycles without performance loss, eliminating filter replacements and drastically reducing 10-year operational costs.
✔ High-Efficiency Filtration + Sterilization – ≥98% single-pass efficiency for particles ≥0.5μm, coupled with a >99% sterilization rate.
✔ Ultra-Low Resistance – <10 Pa resistance (at 1 m/s airflow), reducing HVAC energy consumption.
✔ Safe & Sustainable – Zero ozone emissions, compliant with multiple safety and environmental certifications.
Extensive lab testing by Besin confirms that the ultra-micro electrostatic technology delivers tangible cost and efficiency benefits:
Faster ROI – Savings on consumables and energy lead to quick cost recovery.
Lower 10-Year TCO –Significant reductions in filter replacement, energy, and maintenance expenses.
Eco-Friendly Operation – The low-resistance design minimizes fan power usage, supporting green manufacturing initiatives.
The technology has passed multiple national certifications and complies with GMP cleanroom requirements, making it ideal for:
API (Active Pharmaceutical Ingredient) purification
Aseptic filling processes
High-humidity environments (RH >90%)
Agri-pharmaceutical crossover applications