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The 21st century has seen a boom in life sciences, with revolutionary breakthroughs in frontiers like vaccines, antibodies, and cell & gene therapy (CGT). As a cornerstone of human health, biotech and pharmaceuticals rely heavily on critical filtration technologies to advance innovation.

LOONG Filtration’s solutions are deeply integrated across key stages of drug development and production:
  • LVP
  • Buffer Preparation
  • Facilities Water

Our filtration materials are FDA-compliant and meet USP biosafety standards, while our cleanrooms adhere to ISO 9001 and cGMP guidelines. From sterile raw materials to aseptic production environments, every detail is engineered to ensure product integrity and safety.
 
We empower you to accelerate process scaling, shorten time-to-market, boost production efficiency, and cut costs—turning scientific breakthroughs into life-changing therapies faster.

LVP

 Absolute Sterility Assurance
Thorough removal of bacteria, pyrogens, and particles while accurately preserving active ingredients, ensuring sterility, safety, and compliance of large-volume injectables.
 Zero-Defect Quality Stability
Effectively prevents precipitation and visible particles, avoids product deterioration, and guarantees clarity and long-term stability for every batch.
 High Product Yield
Optimized filtration processes significantly reduce drug adsorption and residue, maximizing the conversion of bulk solution into qualified final products.
 Maximum Production Efficiency
High-flow filtration systems enable rapid fluid processing, shorten production cycles, and speed up filling—getting medicines to market faster.

BUFFER PREPARATION

 Absolute Sterility Assurance
Effectively removes bacteria and endotoxins to ensure buffer sterility and compliance, protecting the entire production process from microbial contamination.
 Exceptional Clarity and Consistency
Eliminates particulates and impurities to guarantee buffer solution clarity, ensuring batch-to-batch reproducibility and reliable downstream performance.
 High Recovery Rate
Minimizes buffer retention and adsorption, maximizing solution utilization and reducing raw material waste for greater cost efficiency.
 Uninterrupted Production Flow
High-throughput filtration enables rapid preparation and on-demand supply of buffers, preventing bottlenecks in bioprocessing workflows.

FACILITIES WATER

 Absolute Purity & Compliance
Effectively removes endotoxins, microorganisms, and contaminants to consistently produce water that meets strict pharmacopeial standards (e.g., USP, EP), ensuring product safety and regulatory compliance.
 Uninterrupted System Reliability 
Robust filtration prevents microbial proliferation and biofilm formation, safeguarding the purified water (PW) and water for injection (WFI) system integrity for continuous, dependable operation.
 Reduced Operating Costs
High-efficiency membranes and optimized processes lower energy consumption, minimize cleaning frequency, and extend system lifespan, delivering significant cost savings.
 Simplified Validation & Maintenance
Consistent filter performance and integrity testability streamline quality assurance processes, reducing validation burden and minimizing downtime.

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Address: 19.Building 12, No. 42, Tianhe Road, Donghu Street, Linping, Hangzhou, Zhejiang,P.R. China

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