Pharmaceutical Contained Aseptic Transfer Valves: ChargePoint AseptiSafe® Brochure

• Perform aseptic transfers that maintain critical area integrity.
• Reduce risk of cross contamination with closed transfers that limit manual intervention.
• Meet GMP and product quality requirements.
• Remove high air class control areas and cumbersome PPE.
• Process toxic powders, ensuring the safety of your personnel and a dust free environment.
• Maximize yield transferring poorly flowing and high value product.
• Prior to the transfer process the Passive unit/ container is pre-sterilized outside of the process.
• This is normally completed in an Autoclave and the critical interface that will be later exposed to the production area can be sealed with a GMP Cover.
• Each half of the valve contains one half of a butterfly valve disc. Each unit is sealed and cannot be opened unless they are docked together

Solutions to meet critical area set up and required sterility assurance
Two alternative methods of sterilizing the product contact and sealing faces of the valve are available to meet the critical area and process set up. In both cases, patented split-valve technology will ensure a closed environment at the point of transfer and throughout the handling and storage process.