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Turnkey Cleanroom Project with Integrated Design Production and Installation
| 브랜드 이름: | SHP |
| 모델 번호: | 맞춤형 |
| MOQ: | 50 평방 미터 |
| 가격: | $500.00/square meters 50-499 square meters |
| 지불 조건: | 신용장, 티/티 |
| 공급 능력: | ≥1 세트 |
상세 정보
원래 장소:
중국
인증:
CE、ISO
상태:
새로운
적용산업:
제조 공장, 식품 및 음료 공장, 화장품, 전자 제품, 실험실, 클린룸, 무진 작업장, 병원
기계 시험 보고서:
제공
핵심 구성 요소의 보증:
1년
청결:
클래스 100 ~ 클래스 100,000
헤파 필터:
99.995%@0.3um 또는 필요에 따라
핵심 단어:
턴키 솔루션 클린룸
애플리케이션:
전자제품, 식품, 병원
자격증:
CE ISO
품목 이름:
GMP 무균실
재료:
암면 샌드위치 패널 또는 중공 유리 마그네슘 샌드위치 패널
작업 범위:
건설, HVAC, 전기, 프로세스 배관
포장 세부 사항:
나무 케이스, 아연 도금 강철 팔레트, 플라스틱 필름
공급 능력:
≥1 세트
강조하다:
turnkey cleanroom project
,integrated cleanroom design
,cleanroom installation service
제품 설명
Product Overview ——Turnkey Cleanroom Project with Integrated Design Production and Installation
A cleanroom can be customized to match different space sizes, layout needs, and cleanliness requirements. From wall panels and doors to windows, lighting, and air handling systems, every part can be designed to create a practical and efficient clean space.
Cleanroom Description
| Application | Pharmaceutical | Lab | Electronics |
| Cleanliness | China class 100 to 100000 | ISO 5 to 8 | EU B to D |
| Scope |
Structure part; Partition and ceiling panel; door and window,epoxy. |
HVAC part; AHU and chiller; Ducting and piping. |
Electrical part; Lamp,switch and socket; Distribution cabinet. |
| Service | Design and production | Construction and test | Validation and training |
| Wall/ceiling panel | Machine-made or Hand-made sandwich board |
| Clean room equipment | Air shower,FFU,Pass box,Laminar flow cabinet,hepa box |
| Cleanliness | Class 100-100000 |
| Purification system | HVAC, or AC conditioner+FFU |
| Floor | PVC anti-static floor or epoxy-based coating |
| Other addessores | stalinite window,LED panel light,Door,Hand wash sink,storage/shoe cabinet etc |
| Service | Design,manufacturing,construction |
Features at a Glance
1. Air Filtration & Contamination Control
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Utilize high-efficiency particulate air (HEPA) or ultra-low penetration air (ULPA) filters to remove airborne particles (down to 0.1 microns) and contaminants, maintaining the specified particle count per cubic foot/meter.
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Control air exchange rate (ACH) to ensure continuous air renewal, preventing the accumulation of dust, microbes, and volatile organic compounds (VOCs).
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Maintain positive or negative air pressure relative to the surrounding environment to prevent external contamination from entering (positive pressure) or contain internal contaminants (negative pressure, e.g., for biohazardous applications).
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2. Environmental Parameter Regulation
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Precise temperature control (typically 20-24°C / 68-75°F) to ensure stability for sensitive processes, materials, and equipment.
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Humidity control (usually 40-60% RH) to prevent moisture-related issues such as condensation, electrostatic discharge (ESD), and material degradation.
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ESD control measures (e.g., anti-static flooring, grounding equipment, ESD wristbands) to protect electrostatic-sensitive devices (ESDs) from damage.
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3. Process Support & Operational Safety
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Provide a controlled workspace for critical manufacturing, research, or testing processes (e.g., semiconductor fabrication, pharmaceutical production, medical device assembly, laboratory research).
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Facilitate sterile operations (for pharmaceutical and medical fields) by minimizing microbial contamination through air filtration, surface disinfection, and controlled access.
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Incorporate gowning rooms, air showers, and pass-through chambers to ensure personnel and materials enter the cleanroom without introducing contaminants.
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4. Compliance & Quality Assurance
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Meet international industry standards (e.g., ISO 14644 for cleanroom classification, GMP for pharmaceutical manufacturing) to ensure product quality and regulatory compliance.
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Support regular monitoring and testing (particle count, air pressure, temperature, humidity) to verify and maintain cleanroom performance.
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Prevent cross-contamination between different cleanroom zones (e.g., different classification levels) through dedicated airflow systems and access controls.
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5. Equipment & Material Protection
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Protect sensitive equipment (e.g., microscopes, semiconductor tools, bioreactors) from dust and contaminants that could affect performance or lifespan.
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Preserve the integrity of raw materials and finished products by preventing contamination during storage, handling, and processing.
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Products Description
Pharma,Biotech&Labs
With today's new regulations and growing concernforpublicsecurity,pharmaceutical,biotech and medical device industries need to maintain and upgrad their facilities in order to meet new requirements and regulations.SHP's in-house experts have the necessary experience in designing building and installin cleanrooms and enclosures to be compliant with new standards.And our knowledge and experience cove a wide range such as infusion production, tablet making and vaccine project,etc.
Electronic,Semiconductors&High-tech Industry
SHP designs,manufactures and installs cleanrooms for the semiconductor and high-technology sectors,from optics,photonics to the assembly of electronic components.In these induatries,products are often very sensitive to airborne particulates and must be manufactured in a controlled environment.Inaddition,these industries often require the use of ultra-precise and costly equipment that must be housed and operated in a location where temperature and humidity are maintained at a specific level.
Hospital
SHP designs and installs cleanrooms that can work well for hospital and pharmaceutical applications and are of high quality to meet stringent cleanroom standards.High levels of environmental control are required to protect patients' health.SHP constructs cleanrooms that can incorporate existing structures or stand freely and offers a high level of environmental control including static,pressure,contamination,and humidity control can be designed to comply with even the most stringent medical standards.
Food Processing&Packaging
Food Processing is an industry where product safety,quality,and integrity are paramount.Assuch,cleanrooms are vital in the food manufacturing industry to ensure food product quality and to adhere to GMP(ISO) standards and requirements,In food manufacturing,cleanrooms must generally meet ISO Class 6 standards.We offer a variety of options to meet your application's specific needs,from highly controlled HardWall cleanrooms that can be built to comply with the most stringent classification to SoftWallcleanrooms with a high degree of flexibility thatwork well for food storage and similar uses.
Manufacturing Industry
Authoritative documents such as ISO 14644 provide no specific instructions regarding activities carried out in other manufacturing industry such as medical device enbvironment.Broadly,medical device manufacturing is conducted in an ISO Class 5 cleanroom(Feb.Class 3),while medical device packaging is conducted in an ISO Class 7-8 cleanroom.Guaranteed completion and final compliance testing are among the reasons SHP is a trusted ally of enterprise in this area as well.
