Industry Pain Points
Pharmaceutical manufacturing demands exceptionally stringent environmental cleanliness and must strictly comply with GMP and ISO 14644 standards. Different zones—such as Grades A, B, C and D—impose graded control requirements on indicators including airborne particles and microorganisms. Meanwhile, the entire process chain—from raw-material weighing through to packaging, covering aseptic production, filling and lyophilization—must guard against contamination risks. Real-world operating conditions frequently involve customized requirements, making it difficult for conventional generic solutions to simultaneously balance compliance, flexibility and long-term stable operation.
The LANSIR Solution
LANSIR provides a complete set of customized air-purification solutions and a product portfolio covering every stage—fresh-air supply, recirculation, exhaust and local purification. Main products include: AHU coarse/medium-efficiency filters, ceiling air-supply outlets, high-efficiency (HEPA) filters, self-contained fan filter units (FFU), exhaust chemical filters, laminar flow hoods and high-temperature-resistant (HT) HEPA filters. From R&D and manufacturing through to installation and after-sales, we always put the customer first, flexibly adapting to different cleanliness grades (A/B/C/D) and the needs of sterile and non-sterile zones to ensure reliable operation and meet individual operating-condition requirements.
Application Scenarios
Biologics and sterile drug-product manufacturing; oral solid dosage (OSD) manufacturing; active pharmaceutical ingredient (API) production; laboratories and biosafety; and medical-device manufacturing
