High containment powder transfer valve
Ensure high containment for potent powders in your production line, reducing contamination risks and maximizing yield without cumbersome protective gear.
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.
Benefits
- Ensures operator safety with high containment levels validated to <0.1 µg/m3.
- Streamlines production by eliminating the need for secondary containment systems and PPE.
- Supports GMP compliance, enhancing product quality and regulatory adherence.
- Increases yield by facilitating the transfer of poorly flowing and high-value products.
- Integrates seamlessly into existing production lines, supporting both batch and continuous processes.
- Applications
- Semi-solids,High value products,Pharmaceuticals,Battery powders,Granular materials,Formulated blends,Powders,Apis,Intermediates,Tablets,Excipients,Reagents,Pharmaceutical powders,Coating materials,Capsules,Liquids
- End products
- Antihistamine syrup,Lactose-based pharmaceutical blends,Vitamin d coating materials,Anticoagulant reagents,Lithium-ion battery powders,Polyethylene glycol excipients,Glucose granules,Rosuvastatin calcium tablets,Albuterol solution,Pharmaceutical grade talc,Ibuprofen capsules,Ibuprofen suspension,Duloxetine intermediates,Amorphous silicon oxide powders,Cough syrup formulations,Antiretroviral tablets,Protein powder supplements,Paracetamol tablets,High purity active pharmaceutical ingredients (apis)
- Steps before
- Dispensing,Milling,Drying,Mixing,Wet/dry granulation,Sieving
- Steps after
- Filling,Coating,Tablets / capsules,Sampling
- Input ingredients
- non-sterile API,formulation ingredients,powder,reagents,semi-solid,intermediates,granular,excipients,suspension,formulated blends,raw materials,liquid
- Output ingredients
- powder,formulated blends,tablets,capsules,processed materials
- Market info
- Chargepoint Technology is known for its expertise in designing and manufacturing high containment and sterile transfer solutions for pharmaceutical and biopharmaceutical industries, particularly in powder containment and aseptic transfer systems.
- Containment performance
- Down to 0.1 µg/m³
- Containment performance
- <0.1 µg/m³
- Compliance guideline
- ISPE SMEPAC
- Operation type
- Split butterfly valve sequence
- Material transfer type
- Powder
- Containment method
- Sealed docked units
- Optional extraction process
- Higher performance available
- Application stages
- All stages of the production process
- Working Mechanism
- Split Butterfly Valve Technology
- Integrated Steps
- Docking,Locking,Transfer,Sealing
- CIP/SIP Capability
- Optional High Performance Extraction Process
- Batch vs. Continuous Operation
- Batch
- Automation Level
- Manual / PLC
- Contamination Risk Reduction
- Validated Containment Performance
- Operator Protection
- High Containment Levels
- Pressure Stability
- Sealed Interface
- Yield Maximization
- Transfers Poorly Flowing and High Value Products
- Changeover Time
- Minimal Due to Design
- Density/particle size
- 0.5–2.5 g/cm³ / 50–1000 µm
- GMP Compliance
- Yes
- ISPE SMEPAC Guideline
- Validated
- FDA compliance
- Potentially yes,based on GMP requirements
- ATEX certification
- Potentially suitable
- Valve Design
- Split Butterfly Valve
- Compact footprint
- Yes
- Discharge method
- Sealed transfer
- Valve Size
- Varies by model
- Material
- Stainless Steel
- Sealing Method
- No additional seals required
- Connectivity Interface
- Active and Passive docking
- Control panel type
- Manual / PLC / HMI
- Integration possibilities
- Seamless with existing setups
- Footprint
- Compact and space-saving
- Valve sizes
- Customizable per requirement
- Material finish
- Stainless steel options available