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ASTM International, 11/01/2016
Publisher: ASTM
File Format: PDF
$34.00$68.00
Published:01/11/2016
Pages:10
File Size:1 file , 280 KB
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1.1 This document provides guidance on the assessment of risks to product quality within and related to PAT processes in the pharmaceutical industry. It addresses those risks to product quality arising from, associated with, identified by, or modified by the implementation of PAT in pharmaceutical development and manufacturing for primary, secondary, and biotech sectors of the industry. It does not replace those assessments of risk currently undertaken by pharmaceutical companies, but is, rather, an additional component focused specifically upon the evaluation and design of PAT processes. See Practice E2474, Guide E2500, and ICH Q8.
1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Note that safety in this context refers to operational and operator safety, not to patient safety.
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Standard Practice for Determination of 2 % Secant Modulus for Polyethylene Geomembranes
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ASTM Book of Standards Volume 11.05 Environmental Assessment, Risk Management and Corrective Action
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Standard Practice for Determination of Contamination in Recycled Poly(Ethylene Terephthalate) (PET) Flakes and Chips Using a Plaque Test
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