The integrity of your manufactured products relies on proven cleaning processes and reliable analytical methods. Our specialized service ensures that your cleaning programs are effective, consistent, and fully supported by rigorous data. we validate the analytical techniques used to measure residues and determine scientifically sound limits, providing the necessary assurance for regulatory compliance and product quality across your GxP
Documented proof that analytical procedures are suitable for their intended purpose (eg., accuracy, precision, linearity, limit of detection/ quantitation). Essential for measuring cleaning residues.
Development and remediation of cleaning validation master plans and protocols. Addressing regulatory gaps and ensuring compliance with FDA, EMA, and other guidelines.
Utilizing data and scientific principles to refine cleaning procedures, potentially reducing cycle times, chemical usage, and resource consumption while maintaining efficacy.
Scientifically determining the efficiency of residue recovery from equipment surfaces. This critical data is used to correct analytical results and calculate accurate final residues levels.
Expertise in calculating the Maximum Allowable Carryover (MACO) or Health Based Exposure Limits (HBELs) for compounds, providing scientifically justified and defendable cleaning limits.
Preparing all validation documentation and data to ensure readiness for regulatory inspections and internal/external audits, establishing a defensible cleaning history.