Controls and Transfers Powders Safely

The Sterisplit Split Butterfly Valve from Hanningfield offers a reliable solution for handling and transferring pharmaceutical, nutraceutical, and chemical powders. Designed to meet stringent cGMP and EHEDG standards, this valve features a unique two-part design, allowing for controlled powder flow while maintaining a clean external surface. Its stainless steel construction ensures durability and resistance to corrosion, while translucent silicone, EPDM, and FKM seals offer compatibility with various substances. Applications span paracetamol tablets, protein supplements, and even dangerous substances like pesticides and explosive powders. Integrating seamlessly into existing production lines, the Sterisplit supports both manual and continuous operations, ensuring precise dosing and efficient containment. With certifications such as FDA compliance and ATEX safety, and a CIP-ready design for easy cleaning, this valve is customizable to suit diverse industrial needs.

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Facilitates Effective Powder Discharge

ChargePoint’s Vibratory Collar is a key tool for optimizing powder discharge in industries such as pharmaceuticals and fine chemicals. Designed to assist powder flow from rigid ChargeBottle® containers, it uses pneumatic power and a simple over-center latch system to securely facilitate powder release. This collar supports operations by enhancing the consistency of product flow, crucial for pharmaceuticals like tablets and APIs, or battery industry materials such as lithium-ion powders. Available in 25L and 10L sizes with durable 304 or 316L stainless steel construction, it offers flexibility and durability. The Vibratory Collar integrates seamlessly into existing production lines with options for manual or batch operations and is ideal for various scales of powder handling equipment.

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Transfers and Contains Pharmaceutical Powders

The Single Use Split Butterfly Valve Passive by ChargePoint Technology is an innovative solution specifically designed for the seamless transfer of pharmaceutical powders, ensuring stringent containment and sterility. This disposable valve integrates into your production line as the passive mating half of the ChargePoint Split Butterfly Valve system. It excels in aseptic processing, eliminating cleaning and maintenance burdens while maintaining high containment levels. Constructed from FDA and USP Class VI compliant plastics, it accommodates both sterile and non-sterile applications. Perfect for pharmaceutical, biotech, and chemical industries, this valve supports various applications, including powder transfer, chemical synthesis, and solid dose formulation. Supplied sterilized and ready for use, the valve ensures efficiency, supporting compliance with GMP standards. Its design allows for a swift, secure connection during powder handling, making it a practical choice for facilities prioritizing speed, safety, and sterility.

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Transfers and Contains Potent Powders Safely

The ChargePoint PharmaSafe® Containment Valve range is engineered for precise and safe powder transfers, offering pharmaceutical manufacturers and biotech companies an industry-leading solution for managing potent materials. Utilizing split butterfly valve technology, it facilitates secure docking of active and passive units, ensuring contamination-free transfer of APIs, excipients, and formulated blends. This valve’s design supports a wide range of applications, including vessel charging, mixing, and granulation, making it integral across pharmaceuticals, biotech, chemical, and even battery industries. The PharmaSafe® pro and excel models provide enhanced containment with vacuum or low-volume extraction options, achieving containment levels down to <0.1 µg/m3, validated per ISPE SMEPAC guidelines. Designed to integrate seamlessly into continuous and batch processing, these valves offer a robust solution compliant with GMP and stringent regulatory standards. Constructed for durability, they enable efficient cleaning and maintenance, supporting high throughput and enhanced safety.

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Ensures Dust-Free Powder Transfer

The Split Butterfly Valve DiscLock™ from ChargePoint Technology is engineered to provide high-containment powder transfer for your pharmaceutical and chemical production needs. This system utilizes a patented DiscLock™ mechanism, ensuring a robust disc-to-disc containment seal that maintains a compact footprint in your processing line. Ideal for dispensing and vessel charging of pharmaceuticals, chemical reagents, and raw materials, it effectively handles powders, granules, and semi-solids with minimized risk of cross-contamination and operator exposure.

Integrated automation allows seamless operation under high-containment conditions, with containment performance solutions capable of achieving levels down to 0.1µg/m³. The system complies with ISPE SMEPAC guidelines, offering GMP and product quality assurance. Constructed from stainless steel for enhanced durability and chemical resistance, it supports low-maintenance operations and integrates easily into existing setups, with options for CIP systems and adjustable configurations to meet specific processing requirements.

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Controls and Contains Flow in Industrial Processes

The PuroVaso® PuroValve™ from ChargePoint Technology is a plastic butterfly valve engineered to enhance flow control and isolation in critical industrial processes. Manufactured from FDA-conforming, high-performance engineering plastics, this 500g valve stands out for its quick-release design, allowing tool-free disassembly in seconds for easy cleaning. Ideal for pharmaceutical, biotech, and battery industries, it supports the handling of powders and solids like paracetamol tablets and lithium-ion battery cathodes. Equipped with an anodised aluminium handle featuring an index for precise positioning, the PuroValve™ seamlessly integrates into pre-processing, processing, and cleaning operations. Its lightweight construction and manual operations make it a practical choice for improving operational efficiency while maintaining sterility assurance and containment.

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Facilitates In-Place Cleaning and Sterilization

The Active Cleaning Cap from ChargePoint Technology excels in enhancing the cleanliness and sterility of transfer valve systems within the challenging environments of pharmaceutical and chemical manufacturing. This equipment offers unique features such as a GMP-compliant design that maximizes exposure of the active unit’s surface area during the cleaning cycle. With a special sealing methodology, it eliminates traditional seat/disc components, ensuring thorough decontamination and reducing cross-contamination risks. Ideal for applications in sterility assurance and powder containment, it supports processes like WIP, CIP, and SIP. Its compatibility with active pharmaceutical ingredients and hazardous chemical powders makes it vital for maintaining a controlled environment in aseptic manufacturing. Available in various configurations and materials like 316L stainless steel and optional A22, this system offers both manual and batch operation flexibility. Its integration capability within existing systems is seamless, providing manufacturers with a reliable solution for comprehensive in-place cleaning and sterilization.

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Opens Passive Valves for Sterilization Process

The Autoclave Passive Opener, by ChargePoint Technology, is engineered to effectively sterilize passive valves and integrated containers in pharmaceutical, biotech, and chemical industries. It stands out by securely opening passive units without requiring a full active assembly, using a hygienic tri-clamp option for secure docking within an autoclave. The design maximizes exposure of product contact surfaces through a unique ‘cruciform’ disc configuration, ensuring comprehensive sterilization during cleaning cycles. Compatible with valve sizes DN50 (2”) to DN200 (8”), this opener is constructed from corrosion-resistant PEEK and 316L or Alloy 22 materials, with FKM or FFKM seals for optimal chemical resistance. It supports GMP-compliant operations, allowing efficient drainage of condensate to maintain sterility assurance. Suitable for sterilization and containment of APIs, sterile powders, and biologic materials, it integrates seamlessly into manual and batch operations for demanding sterility and containment solutions.

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Absorbs Docking Forces and Accommodates Misalignment

The Compensator from ChargePoint Technology is a robust solution designed to enhance the docking processes in powder handling systems. This device excels by absorbing the forces generated during the docking of active and passive units, reducing wear and potential damage. Ideal for pharmaceutical, chemical, and battery industries, it ensures precise alignment, even under challenging conditions. Integrating seamlessly with existing systems, it connects directly to active units or via Tri-Clamp connections, accommodating valve sizes from DN100 (4”) to DN300 (12”). Constructed with 316L stainless steel and EPDM, the Compensator offers exceptional durability and compatibility with a wide range of materials. This is crucial for operations involving sensitive products like APIs, sterile powders, and battery components. By facilitating shock absorption and misalignment accommodation, this device contributes significantly to operational efficiency and equipment lifespan, making it an invaluable addition to any processing line.

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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.

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