Delivering optimum manufacturing environments requires the design and build of cleanroom facilities that meet stringent standards in the production process of pharmaceuticals. However, scalable manufacturing methods, compartmentalised production and sterile and non-sterile classifications provide manufacturers with a number of options and subsequent efficiencies of operation.
As the industry looks to drive efficiencies through the value chain — including the supply and manufacturing process — the race is on to find an energy efficient procedure for controlled environments that maintains the right quality and temperature at the lowest possible price. Michael Rodd, Chief Sales Officer at M+W Products, puts the role of the cleanroom in the pharmaceutical sector into context and signposts how future practice is changing the traditional concept of cleanroom procedures as the cleanroom technology industry pushes the frontiers of controlled environments and scalable solutions, whilst demanding cost-effective and greener results.
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