VHP LTS-V is a large production sized sterilizer and is designed to sterilize the surfaces of packaged biologic drug delivery devices and other temperature sensitive medical devices. This unit allows manufacturers to control the sterilization process on-site with a short cycle time. ISO 14930 Process Validation Services is a new service being offered by STERIS to be able to provide full process validation and required laboratory services related from feasibility testing to validation per ISO 14937 standard for the pharmaceutical and medical device industry. This way STERIS can provide valuable help to our Customers as an expert validation service offering, that is highly important in meeting regulatory requirements and implementing VHP sterilization process to the medical device or drug delivery device manufacturing process. Watch the video below for more information on the STERIS VHP^® LTS-V Low Temperature Sterilization - ISO 14937 Process Validation Services.

Learn more about the VHP LTS-V or request a quote for your facility.  In the video below, learn more about the features and benefits of the VHP LTS-V.