Clean Room Door:
Form a complete set for all levels of clean room, purification room, dust-free room, trailer and other places using color plate partition. Around double sealing, thermal insulation, heat insulation, sound insulation. Color plate or stainless steel plate can be used to customize different size of clean door, locks, color of color steel, door strip, etc can be configured in accordance with the requirements.
| Product Name |
Clean Room Door |
| Material |
Stainless Steel 304/316(L) or polyurethane sandwich panel |
| Size |
Single Door |
Double Door |
|
W:700mm*H:2100*T:50 mm
W:800mm*H:2100*T:50 mm
W:900mm*H:2100*T:50 mm |
W:1200mm*H:2100*T:50 mm W:1500mm*H:2100*T:50 mm W:1800mm*H:2100*T:50 mm |
| Observation Window |
Available |
| Window size |
5mm thickness tempered glass 400mm*600mm/400mm*400mm,right or round corner |
| Window Frames |
Aluminum Profile |
| Surface |
Electrostatic Powder Coating Processing |
| Color |
Blue or customized |
| Core |
Paper honeycomb/Rock Wool/PU |
| Open Method |
Swing or automatic(optional) |
| Seal |
3m industrial tape seal, neutral silica gel |
| Dry |
Inner adding molecular sieve desiccant |
What are the requirements for GMP doors?
GMP (Good Manufacturing Practice) doors are designed and installed to meet the stringent requirements of cleanrooms, laboratories, and other controlled environments in pharmaceutical, biotech, medical device, and food manufacturing industries. GMP doors play a critical role in maintaining the air quality, hygiene, and contamination control within these facilities.Compliance with local and international regulatory standards, such as those set by the FDA (US Food and Drug Administration), EU GMP, or WHO (World Health Organization), is also essential for GMP doors.
Sz pharma door manufacturers offers doors systems adapted to your production prozess, taking account of the space available and how frequently the clean rooms are. During the engineering process we are considering the most economical system. the door systems are as revolving doors, swing door, sliding door and rolling gate available. Fulfilling the most exacting demands of clean room classes, the door panel can be set under reduced pressure. This reduces the particle emission.
The key requirements for GMP doors include:
Material: Doors should be made from non-shedding, easy-to-clean materials that can withstand rigorous cleaning procedures and chemical disinfectants. Common materials include stainless steel, PVC, or high-grade plastics.
Sealing: The pharmaceutican doors must have an effective sealing system to minimize the passage of particles, air, and microorganisms. This typically includes tight-fitting frames with gaskets or automatic bottom sweeps to create an airtight seal when the door is closed.
Durability: Doors should be durable enough to withstand frequent use and abuse without compromising their integrity or functionality. They need to be impact-resistant and able to maintain their shape over time.
Surface Finish: Smooth surfaces are necessary to prevent particle accumulation and facilitate cleaning. No cracks or crevices should be present where contaminants could hide.
Hardware: Pharmaceutical door hardware such as hinges, handles, locks, and closers must be designed for minimal particulate generation and easy cleaning. Often, they are made from corrosion-resistant materials like stainless steel.
Airlocks: In some cases, GMP doors may be part of an airlock system to control air pressure differentials between rooms, preventing cross-contamination.
Visibility: Clear vision panels might be required for safety purposes or to allow visual monitoring while minimizing the number of seams and gaps.
Fire-Rating: Depending on the facility's fire safety plan, GMP doors may need to meet specific fire-resistance ratings.
Automation: Automated systems for opening and closing doors can reduce human contact and potential contamination. These often include touchless activation sensors.
Documentation: All aspects of the door's design, installation, and maintenance should be documented according to GMP guidelines to ensure traceability and compliance.
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