Premier Pharma Cleanroom Solutions & EPC Engineering
AIPURE is a global leader in turnkey pharmaceutical cleanroom solutions, specializing in design, construction, and validation services compliant with US FDA, EU GMP, and WHO standards
The Evolution of Excellence: From Foundation to Global Leadership
The Birth of AIPURE: A Strategic Alliance for the Future
AIPURE represents a powerful new chapter in the life science engineering industry. Formed through the strategic merger of AIPAK—a globally recognized leader in pharmaceutical processing and packaging—and KSP (KeShengPeng)—an elite high-tech enterprise specializing in sophisticated cleanroom engineering—AIPURE combines decades of commercial experience with world-class technical execution.
By integrating the pharmaceutical machinery expertise of AIPAK with the complex engineering and purification mastery of KSP, AIPURE now offers a seamless, 360-degree ecosystem. We provide our global partners with a unified source for conceptual design, high-performance equipment, and turn-key cleanroom construction, all under one prestigious brand.
Our Legacy of Engineering Mastery
Since our foundational roots in 2004, the AIPURE team (formerly KSP) has established itself as a pioneer in integrated cleanroom solutions. We specialize in high-precision cleanroom design, advanced HVAC system engineering, and certified process piping (ASME B31.3). Our core strength lies in our deep understanding of regulatory expertise, with over 20 years of experience in delivering GMP-compliant facilities that exceed international standards.
Technical Capabilities & Global Standards
At AIPURE, we push the boundaries of pharmaceutical automation and intelligence. Our combined engineering team delivers cost-effective, high-performance systems for sterilization, water treatment, and integrated EMS/BMS environmental monitoring. Every project we undertake—from sterile injectable lines to high-containment BSL-3 laboratories—is meticulously engineered to fulfill US FDA, EU GMP, and ISO 14644 requirements.
The AIPURE Promise: Engineering Your Scientific Legacy
We believe a pharmaceutical cleanroom is more than a facility; it is a long-term investment in drug safety and human health. By combining advanced BIM digital modeling with the heritage of professional craftsmanship from KSP and the global service network of AIPAK, we build facilities that operate at peak performance from day one.
Quality is no longer just a standard—it is the unified promise of AIPURE to our global partners.
About Our Company
Professional Pharma Cleanroom Factory, Expert Engineering Team
AIPURE builds on KSP’s cleanroom engineering heritage since 2004 as a specialized high-tech enterprise dedicated to providing integrated turnkey pharma cleanroom solutions. We specialize in the design, construction, and validation of controlled environments for biopharmaceuticals, sterile injectables, and high-containment laboratories (BSL-2/3). With over 20 years of expertise, our team of 200+ technical experts ensures every project meets the most rigorous US FDA, EU GMP, and ISO 14644 standards.
Our competitive edge lies in our BIM-led Digital Deepening and Secondary Design Optimization. By utilizing advanced 3D coordination, we eliminate spatial conflicts and re-verify every utility point—including water, electricity, and process gas—against the equipment general-arrangement drawings prior to fabrication. This digital-twin approach, combined with HVAC energy simulations, significantly reduces both the carbon footprint and operational costs for our global clients.
AIPURE operates a state-of-the-art modular cleanroom manufacturing center, including the newly commissioned Baistent intelligent manufacturing facility. We specialize in the precision fabrication of cleanroom enclosure systems, producing high-quality handmade sandwich panels, airtight doors, and cleanroom vision panels. By leveraging a portfolio of patented technologies in controlled environment engineering, we ensure that every cleanroom component is manufactured with superior airtightness and durability to meet US FDA and EU GMP requirements.
The core of AIPURE’s success is our highly skilled cleanroom engineering team, comprising 206 professional technical and management specialists. Our experts bring over 20 years of collective experience in cleanroom HVAC systems, mechanical and electrical installation (Class I), and process piping (ASME B31.3). We don’t just provide labor; we provide strategic GMP/FDA compliance consultancy to help pharmaceutical and medical device facilities solve their most complex environmental challenges.
Our engineering team brings 20+ years of experience in cleanroom HVAC systems and modular wall panel systems. We utilize BIM to eliminate spatial conflicts, ensuring compliance with EU GMP and ISO 14644 cleanliness standards.
We provide a seamless pharma cleanroom turnkey experience—from conceptual layout and process piping (ASME B31.3) to IQ/OQ/PQ validation and SLA-backed after-sales maintenance.
Why Choose AIPURE ?
At AIPURE TECH, we bridge the gap between complex pharmaceutical processes and high-performance environments. With over 20 years of expertise, we are a leading high-tech enterprise dedicated to providing integrated turnkey pharma cleanroom solutions. We strictly adhere to “Quality First” and “Technical Innovation,” ensuring every project fulfills the most rigorous US FDA, EU GMP, and ISO 14644 standards through meticulous testing and digital-twin validation.
Turnkey Cleanroom Projects
AIPURE provides end-to-end cleanroom EPC services worldwide, ensuring all materials—from handmade sandwich panels to airtight doors—are designed for maximum efficiency and full GMP/FDA/ISO compliance.
Advanced Digital Technique
We utilize unique BIM digital twin technology to eliminate spatial conflicts and perform energy-saving simulations, eliminating clashes in complex API and vaccine facility layouts before construction.
Expert Engineering Team
Our team consists of 206 professional technical and management specialists with decades of experience in cleanroom HVAC, process piping (ASME B31.3), and automation.
Modular Innovation
We significantly reduce construction cycles by shifting 80% of the workload to our factory, using prefabricated cleanroom modules and factory-tested utility valve sets for rapid deployment.
Strict Quality Control
Every cleanroom component undergoes rigorous inspection under our "Sample First" strategy, ensuring dimensional and surface-finish deviations are corrected before shipment.
Professional Validation Service
We offer comprehensive risk assessments and full IQ/OQ/PQ validation services, backed by a SLA-backed 4-hour rapid response team for long-term operational support.
Our Values
At AIPURE TECH, our values are the foundation of every turnkey cleanroom project we deliver. We believe that a high-performance controlled environment is a long-term investment in human health and pharmaceutical safety.
Professionalism: Building Industry Excellence
We continuously collaborate with leading pharmaceutical and medical device manufacturers to refine our engineering craft and technical precision. From sterile injectable lines to BSL-3 laboratories, we provide sophisticated, exclusive solutions that meet the highest international standards of US FDA and EU GMP.
Factory-Driven: Precision Manufacturing
Our advanced cutting-edge technology and expert manufacturing team ensure the highest quality for every cleanroom component. By using factory-prefabricated modules, we strive for excellence and self-improvement to meet the evolving demands of the global life sciences market.
Relation: Customer-Centric Partnership
We put our customers first by maintaining timely communication to understand their process requirements. Our dedicated support team leads every client through a comprehensive risk assessment before project execution, ensuring a seamless and transparent partnership.
Quality & Compliance: A Lifelong Promise
Focusing on quality is the ultimate goal at AIPURE TECH. We believe that by delivering superior cleanroom environments, we help our customers produce safer, more effective medicine. We emphasize rigorous quality control from raw materials to final IQ/OQ/PQ validation and lifelong technical support.
Leading manufacturers across multiple regions trust AIPURE for their most critical cleanroom turnkey projects
Simply fill out the form below, and one of our Pharma Cleanroom experts will be in touch with you shortly to discuss your project requirements!
Expert Guidance: Direct access to senior engineers with 20+ years of GMP engineering experience.
Tailored Solutions: Customized technical assessment for your oral solid dosage, nutraceutical, API or sterile injectable project.
Rapid Response: We guarantee a 4-hour response time to address your most tricky environmental challenges.
