Information has to be made, manually or electronically, throughout manufacture that exhibit that all the ways required because of the described treatments and instructions had been in reality taken and that the amount and quality on the foodstuff or drug was as envisioned. Deviations have to be inve

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Mark Birse will be the Group Supervisor, Inspections (GMP/GDP) and manages a workforce of about fifty Inspectors. Mark joined the MHRA in 2002, having Earlier worked in the pharmaceutical field for more than a decade in a number of roles together with process technologies, new product or service int

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