High containment isolator for toxic and active drug handling
Ensure safe handling and environmental protection while processing highly potent and toxic materials, with customizable isolation solutions that maintain product integrity and operator safety during critical pharmaceutical and chemical operations.
Ensures Containment and Sterile Material Transfer
The High Containment Isolator System from AUSTAR is designed to provide unparalleled protection and sterility for handling high potency and toxic pharmaceutical materials. Utilizing adjustable positive or negative pressure environments, this isolator offers a controlled atmosphere for sensitive operations, ensuring operator safety and product integrity. Equipped with HEPA filters for air inlet and exhaust, it achieves efficient air filtration and laminar flow, crucial for sterile processing. It seamlessly integrates with various material transfer systems, such as Rapid Transfer Ports and split butterfly valves, for secure handling. Ideal for applications in manufacturing pharmaceutical tablets, biopharmaceuticals, and cancer treatment drugs, it supports operations from OEB3 to OEB5 containment levels. The isolator is fully customizable to accommodate specific client needs and is accompanied by AUSTAR’s SMEPAC testing service, ensuring compliance with stringent containment requirements. Constructed with high-quality materials for chemical resistance and durability, it meets GMP and FDA standards, and facilitates easy maintenance through safe filter replacements and ergonomic designs.
Benefits
- Enhances worker safety by isolating high potency and toxic materials.
- Meets stringent OEB3 to OEB5 containment levels, ensuring compliance with safety regulations.
- Provides flexibility with customizable configurations for specific operational requirements.
- Supports efficient sterile processing with HEPA-filtered laminar air flow.
- Streamlines material transfer with integrated systems, reducing risk of contamination.
- Applications
- Pharmaceutical tablets,Fine chemicals,Pharmaceutical powder,Biopharmaceuticals,High toxic materials,Active drugs
- End products
- Cytotoxic drugs,High potency apis (active pharmaceutical ingredients),Cancer treatment drugs,Enzyme preparations,Fine powders for tablet compression,Steroidal compounds,Immunosuppressants,Hormone therapy drugs,Injectable biopharmaceuticals,Antiviral medication powders
- Steps before
- Material transfer,Powder handling,Sterile preparation
- Steps after
- Occupational safety protection,Environmental protection,Sterile filling,Quality inspection
- Input ingredients
- high toxic materials,powder materials,sterile components,highly toxic and active drugs
- Output ingredients
- filtered air,sterile materials,contained materials
- Market info
- Austar is known for specializing in the design and manufacture of engineered-to-order industrial equipment, particularly in the pharmaceutical and biotechnology sectors, offering solutions that focus on quality, innovation, and meeting specific customer requirements.
- HEPA Filter
- Replaceable
- Airflow Type
- Laminar
- Pressure Conditions
- Adjustable positive or negative
- Containment Levels
- OEB3 to OEB5
- Environmental Control
- Closed environment
- Material Transfer System
- RTP,Continuous Bag,Split Butterfly Valve
- Safety Protection
- Occupational and Environmental
- Air Speed
- Designed for sterile process requirements
- Transfer Port Mechanism
- ALPHA-BETA Technology
- Interlocking Mechanisms
- 5
- Airflow pattern
- Laminar flow
- Containment level
- OEB3 to OEB5
- Pressure control
- Positive/Negative adjustable
- Material transfer system
- RTP / Continuous bag device / Split butterfly valve
- Occupational safety
- HEPA filtration and collection
- Closure requirement
- Sterile and closed environment
- SMEPAC testing
- Validated OEL
- Sterile integrity
- SIP enabled
- User operation
- Manual / Semi-automatic / Full automatic
- Density/particle size
- 0.5–2.5 g/cm³ / 50–1000 µm
- OEL Validation
- OEB3 to OEB5
- Machine footprint
- Customizable
- Control panel type
- Ergonomic design
- Discharge method
- Closed system
- Shape
- Glove box isolator
- Feed method
- RTP,continuous bag device
- Isolator pressure control
- Adjustable positive or negative
- Airflow control
- Laminar air flow
- Material transfer integration
- RTP/Continuous bag device/Split Butterfly Valve
- Customized isolation level
- OEB3 to OEB5
- Sterile environment design
- Independently or integrated with other equipment
- Interlocking structure
- Alpha-Beta technology in RTP
- Alpha door handle design
- Ergonomic for glove use
- Sterilization method
- WIP/SIP
- Air filtration
- HEPA filter
- Automation level
- Manual/Semi-automatic/Full automatic
- SMEPAC Testing Service customization
- Tailored validation schemes
- Containment level testing
- Personalized OEL validation