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A review of the recent changes in the FDA's thinking on lifecycle based process validation as published in their long awaited update to the 1987 PV guidance. This presentation provides an overview of the key elements of the draft and looks in particular at the role that verification/CQ can play in supporting these outcomes.
$ 49.00 / € 40.00
Non Member Price:
$ 149.00 / € 110.00
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