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Cleaning Validation Lifecycle – Applications, Methods and Controls

Published: August 2020
Pages: 236

Regulatory agencies expect the development and validation of a compliant cleaning program. This critical activity ensures that the risks of contamination, product carryover, and cross contamination are controlled, minimized, and monitored to safeguard patient safety and product quality.

To get more information about this Guidance Document, please visit the ISPE global site or contact ISPE Shanghai by email at

This Guidance Document is currently not available in Chinese.

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