Isolator (Sterility Test Isolator/Sub-package Isolator)

Sterility test isolator/sub-package isolator system includes the following parts: aseptic isolation operation area, material transfer area, bag-in and bag-out pollutant collection processor, pneumatic sealing system, control system, monitoring system, supporting VHP sterilization system. According to the process function, it can be divided into production type, weighing sampling type and testing type. It is mainly used for aseptic testing, weighing, sampling, sub-packaging, packaging and other processes of preparation products and raw materials.

Isolator (Sterility Test Isolator/Sub-package Isolator)
Isolator (Sterility Test Isolator/Sub-package Isolator)
Isolator (Sterility Test Isolator/Sub-package Isolator)
Isolator (Sterility Test Isolator/Sub-package Isolator)
  • Product Description
  • Technical Features
  • Technical Parameters
  • Optional Systems
  • Application Scenarios
  • Video
  • Product Characteristics

     

                           

     

    1.Two-door transfer technology of sterility test pharmaceutical isolators: to ensure that clean space is not affected by material transfer and personnel operation, and to solve the problem that cleanliness of Class 100 traditional aseptic room can not be maintained continuously.

     

    2. Monitoring system: on-line monitor pressure, temperature, humidity, cleanliness and other operating parameters of isolator, to meet GMP/GLP management requirements.

     

    3. Control system: microcomputer automatic control

     

    4. Adjustable positive pressure and negative pressure: it can meet the requirements of toxic substance protection and prevent pollution.

     

    5. Removable cabin: it is easy to move and can reduce the requirements of external environment and save costs.

     

    ​​​​​​​6. Sterilization mode: ozone or pneumatolytic hydrogen peroxide (VHPS) are available.

3 +

Production Bases

70 +

Successful Projects in 70 Countries

300 +

Loyal Clientele




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Invited to the Embassy of the United Republic of Tanzania in Guangzhou to discuss projects

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Tanzanian Vice President Visits Marya Pharmaceutical EPC Project

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NBA (Zimbabwe National Biotechnology Authority) conducts FAT at MARYA’s Factory

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NOVO NORDISK client Visit

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Clients visit the factory's liquid preparation system

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Argentine client visits for FAT in MARYA



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Services


Full-process Consulting Services

Full-process Consulting Services

Whether you are preparing to build a new pharmaceutical factory, build a cleanroom that complies with local GMP regulations, or purchase pharmaceutical equipment to develop a new production line, whether it is a separate cleanroom or pharmaceutical machine project, or a one-stop solution, Marya's professional teams in the fields of pharmaceutical technical process, process equipment, decoration engineering, HVAC engineering, pipeline engineering, utility equipment, intelligent automatic control systems, project cost and other fields can provide you with full-process technical consulting services, and solve your needs one-on-one.

2D/3D Design Modeling Services

2D/3D Design Modeling Services

Marya project design team is composed of professional CAD and BIM engineers with more than 20 years of comprehensive industry experience and can provide you with comprehensive design services, including but not limited to process layout drawings, technical process charts, 3D models and animations, air conditioning system scheme design, construction drawing design, plant/pharmaceutical machine layout drawings, etc.

Machine Customization Services

Machine Customization Services

Based on the individual needs of clients in different countries, Marya helps you clarify specific needs, match appropriate models, and customize one stop filling solutions for sterile small-volume preparations, large-volume injections, oral liquids/syrups, solid preparations, etc.

Validation Services (FAT/SAT)

Validation Services (FAT/SAT)

Marya will appoint an engineer with rich project management experience as the person in charge, who will be fully responsible for project management and liaison work. After the equipment is manufactured, our engineers and the buyer's representatives will participate in the FAT test. After the equipment arrives at the buyer's site, it will be installed and debugged. After the equipment reaches optimal operation, the buyer will conduct SAT testing and inspection.

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Key words:

Isolator

Sterility Test Isolator

Sub-package Isolator

sterility test isolators

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