Whether a life science company is upgrading their existing premises or building a new facility from scratch, multiple challenges around validation will be faced.
It is essential that all aspects of the facility,utility and equipment that can affect product quality is verified and documented that they operated as intended throughout all expected ranges.
In this case study, our customer, one of the leading medical device manufacturers in the world, were expanding their manufacturing operations to cater for the transfer of 3 different product lines from locations around the world.
Stericycle GxP Solutions provided a team of engineers, who integrated with the in-house engineering team to deliver the project successfully and build a foundation on which all follow on validations were based
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