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Shandong Eagle Pharma Machinery Company (WEMAC) is based in Weifang, a city in Shandong Province known globally as the kite capital of the world. WEMAC was originally established in 1958 as Weifang Medical Equipment Factory and has since grown into a specialized manufacturer of pharmaceutical water systems.
Our work focuses on designing and building equipment for purified water, water for injection (WFI), pure steam generation, and complete storage and distribution systems. These solutions are developed to meet the high hygiene and compliance standards of the pharmaceutical industry.
With decades of experience behind us, we’re committed to providing practical solutions, consistent product quality, and reliable after-sales service. Today, our pharmaceutical water treatment systems are used in more than 40 countries and regions, including the United States, Russia, Egypt, India, South Korea, and Argentina.
At WEMAC, we’ve built a solid foundation in pharmaceutical water treatment systems research and engineering with a team that comprises professionals from over ten fields, including mechanical design and automation, electrical engineering, materials processing, control systems, environmental science, and medical electronics. Thanks to this broad expertise, we handle everything from project planning and system design to manufacturing, installation, and on-site validation, following clear and standardized processes at every stage. We currently have over 260 employees, including more than 50 senior technical experts. Our R&D team includes experienced professionals in pharmaceutical equipment and pressure vessel design. Our manufacturing facility spans 61,700 square meters and is designed to meet the standards of a modern pharmaceutical equipment manufacturing site.
We’ve also established close collaborations with universities and research institutes such as Shandong University and Shandong University of Science and Technology. These partnerships help us stay ahead in product development, focusing on high-quality and sustainable pharmaceutical water systems for the pharmaceutical, electronics, and food industries. Our main products include LDS series systems for water for injection (WFI), RO2+EDI purified water systems, CZQ pure steam generators, along with equipment for storage, distribution, and formulation.
We believe that quality shapes outcomes and that responsibility drives progress. Guided by the core principle of putting life and accountability first, we’re committed to developing pharmaceutical water systems, process piping solutions, and laboratory equipment that meet international standards and deliver consistent performance.
Through continuous innovation and a focus on excellence, we aim to support the advancement of pharmaceutical technologies and contribute to improving global health.
We signed a cooperation agreement with AQUACHEM (USA) for the supply of pressure-type distillation units.
Experts from Kinetics (Germany), specialized in fluid purification, visited our facilities to deliver a technical training session.
From initial design to process manufacturing, we provide tailored and practical solutions backed by decades of industry expertise. Our team knows how to turn complex requirements into workable systems that perform reliably in real-world environments.
Our support team is composed of professionals with hands-on experience in equipment operation and maintenance. In addition to technical knowledge, they’ve received system-specific training, allowing them to respond efficiently and confidently to customer needs.
Every pharmaceutical water treatment system we offer is manufactured using advanced equipment, strict quality control, and detailed inspection procedures. This ensures reliable performance, long-term durability, and peace of mind in regulated production environments.
All our pharmaceutical water systems are developed according to GMP (Good Manufacturing Practice) requirements. Automation design and software development are conducted following GAMP (Good Automated Manufacturing Practice) guidelines to ensure compliance and operational reliability.
We hold the necessary qualifications to design and manufacture both Type I and Type II pressure vessels. This allows us to meet diverse technical specifications while ensuring compliance with national safety standards for pressurized equipment.
We provide complete documentation packages for all stages of equipment qualification and system verification, including DQ (Design Qualification), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), as well as FAT (Factory Acceptance Test) and SAT (Site Acceptance Test).
Please take a minute to confirm your process requirements by completing the MSR™ Microsphere Refiner online questionnaire. Our team will help you select the most suitable solution for purified water, WFI, and pure steam generation.
