Critical Cleaning - Alconox, Inc.: General and Current Good Manufacturing Practice for Finished Pharmaceuticals

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General Cleaner Info: Pharmaceutical Cleaning Validation CAP Residue Detection Methods
Catalog	Users Manual

Tuesday, October 28, 2008

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General and Current Good Manufacturing Practice for Finished Pharmaceuticals

Question:
What part of the FDA Code of Federal Regulations applies to cleaning equipment?

Answer:
The FDA Code of Federal Regulations 21 CFR 211.67 applies to equipment cleaning and maintenance. If you are cleaning pharmaceutical equipment with Alconox brand cleaners, our team of experts can assist you in your cleaning validation. For more information on how the Alconox team of validation consultants can assist in your pharma cleaning validation, e-mail us at cleaning@alconox.com or call us at 914.948.4040. If you need pharmaceutical cleaning validation information, visit our website to view the Alconox Pharmaceutical Cleaning Validation References.

(General and Current Good Manufacturing Practice for Finished Pharmaceuticals)