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Cleaning ValidationCleaning validation ensures that specific cleaning processes consistently clean to pre-defined limits to prevent contaminants (product or cleaning process related) from leaving residues that will adulterate and adversely affect the safety and quality of the next product manufactured. Cleaning validation is documented proof of consistently and effectively cleansing a system or equipment item. We can deliver a complete package from development and execution of engineering studies and protocols for pharmaceuticals and biologics to creation of standard cleaning procedures, logs and training documentation. CapabilitiesPharmaSys has extensive experience in developing defensible acceptance criteria and ensuring the execution is conducted in an orderly manner. Our highly skilled individuals can ensure that equipment-cleaning procedures are removing residues to pre-defined levels of acceptability. Our approach involves:
Created SOPs and methods (analysis and recovery) for cleaning validation studies for:
Drafted, executed sampling and testing cleaning validation engineering studies protocols for:
If you are interested in finding out more about PharmaSys' world-class offerings, complete and submit the form provided below. You will be contacted to discuss your needs and provided with information about how PharmaSys can help you achieve your compliance and validation goals. |
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