The Food and Drug Administration (FDA) defines aseptic processing operations as ones that ensure the commercial sterility of a product, as well as of the product sterilization system (i.e., the hold tube) and further processing equipment (i.e., the filler), the packaging machines, and packaging material.
To facilitate compliance with FDA requirements for aseptic processing, Highland Equipment provides manufacturers with process equipment equipped with automated cleaning and sterilization systems:
- Clean-in-place (CIP) systems
- Sterilize-in-place (SIP) systems
- And much more!
Download our new eBook to learn more about the sterilization of processing equipment and to discover all of Highland Equipments product offerings to meet your sterile production needs.