Wholesale Sandwich Panels Clean Room For Modular Cleanroom
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Product Description:GMP Device Cleanroom Solutions(1) It Is Crucial To Maintain a Contaminant-Free Clean Environment When Manufacturing Devices Such As Biological Implants.This Starts With The Clean Room Design And Management Systems. The Clean Room Design Prevents Outside Contamination, While Regular Maintenance And Sanitation Upkeep Minimize The Risk Of Contamination Originating Within The Clean Room Itself.
(2) Implants That Are Non-Sterile Or Are Awaiting Sterilization Should Be Subject To Purification And Clean Packaging Processes. This Will Allow For Uniformity And Control Over Product Quality. When Constructing a GMP Instrument Clean Room, a Location Should Be Designated For The Packaging Process, And Processes Should Be Implemented To Ensure That Products Avoid Contamination Risk At All Times. For Further Reference, Please See The YY0033-2000 Standards.
(3) Procedures Must Be Developed To Control Environments In Which There Exists a Contamination Risk To Products. This Includes Any Time Personnel Makes Contact With a Product, Including When Products Are Moved From One Location To Another. Features:
International GMP Instrument Cleanroom StandardsInternational Standard: ISO/DIS 14644 Chinese Standards: GB50073, GB50591, GB 50243 American Standards: GMP-97, GMP-98, FS209E Considerations for GMP Device Cleanrooms(1) Carefully consider all construction materials to be used. (2) Thoroughly examine your plans for design, installation, testing and maintenance (3) Do not neglect to consider details--such as placement, size, and model--that concern the air purification system Temperature and Relative Humidity Except for certain special circumstances, the temperature of GMP instrument cleanrooms should be calibrated between 18~28℃,with a relatively humidity of 45-65%. If you find that you are out of range for these standards, consider which instruments in the clean room may be acting as a heat source. Air Velocity, Air Change Rate (ACR), and Static Pressure The air change rate of a clean room is a function of the volume of air circulated into the cleanroom and the area of the clean room.Differences in static pressure result from differences in the the amount of air circulating through the air return vs. exhaust system vents. All of these variables can be adjusted through manipulation of fan speed and/or opening/closing the main vents. These can be adjusted for the entire system or for certain areas depending on the situation. Keeping Out Dust, Bacteria, and Other Contaminants Indications that your clean room may not be up to standard include falling out of standard in basic areas such as temperature,relative humidity and ACR. If these variables are out of standard, it is likely that your cleanroom is contaminated to a degree that is out of standard. Proper calibration of the above conditions forms a sort of "microclimate" that is inhospitable to contaminants such as dust particles and bacteria. Meeting standards is a result of proper maintenance of the cleanroom. Regular, thorough testing is the only best practice, especially in a field where product contamination can lead to serious consequences. Besides designing your clean room, E-Clean can advise on how to implement management systems to maintain your clean room and minimize the risk for contamination.
Technical Parameters
If there are other size requirements, it can be
customized Application Products Biological Science Modular Clean-Room Mainly Engaged In Offering
Full Service For System Clean Room Engineering, Including Product
Manufacturing, Equipment Transport, Construction Control,
Engineering Acceptance Test, Etc. The Engineering Contains 4
Sectors, Decoration, HVAC, Plumbing And Electrical Appliances,
Which Includes The Installation Of Process Pipeline, Water Supply
And Drainage Pipeline And Purifying Ventilation Duct, Power
Distribution Of Purification Product And Process Equipment,
Security Control, Whole Plant Centralized Control, Etc, And Which
Are Widely Used In Food, Electronics, And So On. Biological Science
Modular Clean-Room Has a First-Class Engineering Design Team To
Work From Initial Engineering Design, Further Optimize The Drawings
According To Practical Construction Experience, And Even Customize
For Clients. In The Whole Construction Process, Biological Science
Modular Clean-Room Strictly Follows 4Q Standard To Monitor All
Construction Nodes, Applies 3 Level Control From Plant Construction
To Completion And Uses Advanced Equipment To Precisely Test The
Later Project. The Company Processes Advanced ERP System And
Ensures The Engineering, From Quality To Management, As High As
International Level.
Support and Services:Technical support and services for Clean Room Booth include:
Packing and Shipping:Packaging and Shipping for Clean Room Booth:
Company Introduction
Dongguan Yaning Purification Equipment Co. Ltd was established in year 2011. It is was located in Houjie town of Dongguan City. We are a professional manufacturer of industry purification equipment as well as purification project solution provider.We are ISO 9001 certified enterprise national certified high technology enterprise.
Our main product cover several major categories and more than one hundred models, Our main product include air shower room for person and cargo , clean room , pass box, clean bench, fan filter unit, HEPA filter box, laminar air flow ceiling etc. Our air filter product range from primary level to medium and high efficiency level in great variety types. Our equipment have been widely used in hospital, health care, electronics, medicine, food, precise instruments, aerospace, automobile manufacturing industry and so on.
You are welcome to inquire for any of our products or services at any time. Our Exhibition CE certificate:
FAQ:Q&A of Clean Room Booth
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