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
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