skip to Main Content
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 askispeshanghai@ispe.org.

This Guidance Document is currently not available in Chinese.


Guidance Document License Agreement

The contents of ISPE’s guidance documents, both printed and digital, are protected by law and intended solely for the personal non-commercial use of the individual purchaser. Reproduction of multiple copies of these materials, in whole or in part, for the purposes of commercial distribution is prohibited. Membership discounts are available only to current members and are intended for individual use of the guides, not for resale.

Back To Top