VESTA® Multiport
English, 2.32 MB, 652e, 06/2010
Cost-effective manufacture of high sensitivity products in the pharmaceutical and biotechnology industries requires even more complex processes. This places high demands on the engineering, in particular with regard to the process reliability of the complete plant system. In this connection directives (FDA, cGMP), legal frameworks such as EU regulations, and concepts such as qualification and validation are gaining greater significance. In many cases processes using different operating, cleaning and sterilisation media are often applications in sterile process engineering. At the present time such processes are implemented almost exclusively using diaphragm valves in the form of conventional solutions using individual valves or so-called valve blocks. Conventional solutions with individual diaphragm valves in a welded design are known to be very labour-intensive. As well as being time consuming to assemble the valves, fittings and pipe components used also require greater clearances. Dead spaces with systems of this kind are unavoidable and must be taken into account. While valve blocks with diaphragm valves in a block of solid material are compact they are not totally free of dead spaces. Moreover valve blocks of this type are only ’optimised for draiing’ - complete evacuation of the system is not possible. Large wall thicknesses make systems of this kind require long heating-up times during the sterilisation process. Until now there have been few alternatives to systems using membrane valves for such processes. This gap is now filled by the novel VESTA® Multiport from GEA Tuchenhagen. The VESTA® Multiport fitted with VESTA® sterile valves is designed to have zero dead space and be CIP compliant. It provides for total draining, can be located in the smallest of spaces, and at the same time sets new standards in terms of cost effectiveness.