Cleaning Validation Services
Industry Experience, From Basic Verification to Complex Programs
Verifying that process soils are consistently removed from the manufacturing equipment before the next manufacturing run to ensure that clean, uncontaminated equipment is being used to manufacture products without risk of residual unwanted substances. Whether it’s a small company that wants to implement basic cleaning verification or a large industry partner who requires a complex and robust cleaning validation program, our team of experts apply a common core of quality assurance and compliance principles.
ProPharma Group’s staff is highly-trained and 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.