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Cleaning Validation |
Integrated Analytical Laboratories, LLC (IAL) is a cGMP compliant facility available for developing, validating and performing analytical procedures used in equipment cleaning validation protocols.
IAL has conducted experiments to determine swab and rinse recovery conditions for drug substances and cleaning agents. In addition, IAL has developed and validated methods to quantitatively detect residues and contaminants in swab and rinsate samples. Microbial support for cleaning validation is also available.
If you require rapid response protocols, you can trust IAL to develop the appropriate protocols so that you can quickly validate the cleaning of your non-dedicated process equipment.
Please call our Pharmaceutical and Cosmetic Testing Business Development Department at 973-361-4252 for more information regarding our cleaning validation services. You can also contact us via email at pharminfo@ialonline.com.
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