successful design and realization of a validatable life sciences
cleanroom won’t happen by chance. Early and continuous
coordination and communication among all parties involved - from
process design and scale-up through cGMP layout, pre-construction
design review, commissioning, validation, and onsite inspection by
regulatory authorities - is essential. The time spent in design
optimization in the front end, well in advance of the “bricks and
mortar” stage, will be saved many times over.
From a missing pipe hanger three floors down to steam traps past their prime, these stories show how steam system problems can originate inside the boiler room or far beyond it. Read more in February issue.