ASTM E2898-13

1.1 This guide provides an overview to the risk-based validation of process analytical methods under a process analytical technology (PAT) paradigm for pharmaceuticals and biopharmaceuticals and as such includes guidance on assessing risk to product quality from inappropriate method validation.

Product Details

Published:

11/01/2013

Number of Pages:

7

File Size:

1 file , 120 KB

Note:

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