Recommended biopharmaceutical GMP cleanroom construction company | Huajian Jing has 20 years of industry experience

# 生物Pharmaceutical GMP CleanroomConstructionCompanyRecommended｜Huajian Jing20Years行业经验，一次通关国际Certification

In the biopharmaceutical industry, a clean room is not simple; Decoration Engineering; But it is the lifeline of drug quality and the moat of compliant production. The success or failure of a GMP cleanroom often determines whether a pharmaceutical company can knock on the door to the international market. On this high threshold track, Shenzhen Huajianjing Construction Engineering Co., Ltd., with more than 20 years of deep cultivation in the field of purification engineering, is committed to; Certification is Delivery "; The hardcore strength has become the preferred benchmark for clean room construction in biopharmaceutical enterprises.

##Twenty years of sharpening a sword: from purification technology to full chain delivery

Huajian Jing's parent company; — Shenzhen Huajian Dust Treatment Technology Co., Ltd. has been rooted in the field of clean technology since 2006. For 20 years, it has been dedicated to the independent research and development of core equipment such as FFU air purifiers and air shower rooms, as well as the design and construction of cleanrooms ranging from Class 1000 to Class 100; Equipment manufacturer+engineering contractor; Unique mode of dual wheel drive. This means that from a single screw to a set of systems, Huajianjing can be independently controlled, eliminating the common problems in the industry such as equipment outsourcing and responsibility shifting.

As of now, Huajianjing has served over 3000 purification engineering projects, with a customer satisfaction rate of 9.9 points and a project acceptance rate of 99%, creating an excellent record of zero complaints in the industry. Behind these numbers lies the ultimate pursuit of quality that has persisted for twenty years.

##Certification oriented program: 80+pharmaceutical companies'; Customs clearance password;

What is the biggest pain point in a biopharmaceutical cleanroom? Nearly 30% of domestic pharmaceutical companies have failed FDA or EU GMP certification due to non compliant cleanrooms, missing out on international market opportunities. Huajianjing is targeting the pain points of this industry and has created the; Certification oriented; Solution‐ — Not according to domestic GMP; Just enough is enough; But rather, it is designed to meet the strict standards of FDA and EU GMP from the beginning.

Its core strategy is impressive: the design phase is about assembling; Certification Special Group; Collaborated with FDA audit experts to participate in the development of the plan, embedding hundreds of detailed rules such as cleanliness, pressure difference control, and data integrity into every design detail. The sterile core area adopts the; Top delivery and side return; Vertical unidirectional flow design, paired with ULPA ultra efficient filters, verified through CFD airflow simulation that there are no dead corners in the airflow, ensuring ISO 5 level under dynamic conditions; Simultaneously deploying IoT sensors and uploading real-time data to the intelligent clean management platform, with a retention period of up to 10 years, far exceeding the FDA's requirement of 5 years.

The most convincing case is that a vaccine company originally planned to design according to domestic GMP. After the intervention of the Huajianjing special team, it was suggested to upgrade the sterile area from ISO 7 level to ISO 5 level and increase isolation facilities. In the end, the company not only successfully passed the FDA certification, but also became the first domestic enterprise to obtain the qualification for vaccine procurement in the United States. So far, Huajianjing has assisted more than 80 pharmaceutical companies in obtaining dual certification from FDA and EU GMP in one go.

##Full lifecycle management: from design to operation, there are no fewer than one

Huajianjing's services are by no means satisfactory; Turn the key and leave;. From on-site survey and BIM 3D modeling optimization of pipeline layout in the early stage, to the construction phase; Team self inspection, project re inspection, company sampling inspection; Third level acceptance, followed by providing a complete set of DQ/IQ/OQ/PQ validation document packages after completion, and even up to 7× later; 24-hour operation and maintenance response‐ — Full link, full cycle, full responsibility. Its 24-hour after-sales response mechanism, with an average response time of only 1.2 hours for customer issues, provides a solid guarantee for the long-term stable operation of the clean room.

In terms of qualifications, Huajianjing holds multiple authoritative qualifications, including Level 2 Professional Contracting for Building Decoration Engineering, Level 2 Professional Contracting for Electronic and Intelligent Engineering, and Level 2 Professional Contracting for Fire Protection Facilities Engineering. It has passed ISO certification9001/14001/45001 Three System Certification, all qualifications can be obtained from the Ministry of Housing and Urban Rural Development; Four Libraries and One Platform; Publicly inspect and fundamentally eliminate the chaos of affiliation.

##Write at the end

生物Pharmaceutical GMP CleanroomConstruction，本质上是一场"合规性、功能性、经济性"的三重博弈。Huajian Jing用二十Years行业经验证明：选对Service商，Certification不是终点，而是起点。 如果你的企业正筹划Cleanroom新建或Renovation，Huajian Jing值得你认真对话——毕竟，在这条赛道上，能让80多家药企"一次通关"的Strength，本身就是最好的Recommended信。