Cleaning Validation

ProPharma Group recognizes that cleaning validation is just as important as process validation when it comes to the safety and continued compliance of any manufacturing firm. Here, we have the experience and knowledge to help our clients develop and verify their manufacturing equipment consistently removes process soils before the next manufacturing run to ensure clean, uncontaminated equipment. 

Here, our highly trained staff is experienced in developing and executing cleaning development and cleaning validation master plans and protocols in line with current industry standards. We provide a hands-on approach to help guide our clients through the details of establishing a cleaning master plan, setting residue acceptance criteria, preparing a comprehensive sampling plan and validating and utilizing appropriate qualified analytical methods with sufficient sensitivity for those unique processes and equipment. 
 
In this section, you’ll discover all about Cleaning Validation Guidelines and Cleaning Development. For more information, feel free to Contact Us.
Alfredo Canhoto
Alfredo Canhoto has over 15 years' experience in the biotechnology and pharmaceutical industries providing consulting, compliance, audit and validation engineering services, both domestic and...View full bio