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Analysis & performance
 
Bioanalysis and Pharmaceutical Analysis

Cleaning Validation

Pharmaceutical manufacturers are legally required to prove that the cleaning processes used to remove residues from their production systems are effective and consistent to a high degree of certainty. To achieve this, both effective methods of sampling and highly sensitive and selective analytical methods are needed. We offer:

  • Optimization of sampling (swabbing techniques, rinsing protocols, etc.)
  • Development of appropriate sample preparation methods
  • Selection of sensitive and selective analytical methods (e.g., LC/MS or GC/MS), tailored to your cleaning process
  • Development of validated methods in accordance with international standards
  • We have a GLP - Good Laboratory Practice certificate.
Cleaning validation