Mobile search icon
Services >> Facility and Process Control >> Cleaning Validations

Cleaning Validations

Pharmaceutical industry

Cleaning validations are a critical part of your production process ensuring that the quality of your next product manufactured in the same clean/aseptic area is not compromised by waste from previous products and prevent cross-contamination. EBPT-NL can support you with our cleaning validation services, but we can also assist you in: 

 

  • Evaluation of critical risks for cross-contamination during manufacturing
  • Calculation of allowed residue levels on manufacturing equipment
  • Development and validation of analytical methods to detect cross-contaminants
  • Design of cleaning programmes
  • Sampling according to predetermined sampling plans
  • Analysis of samples taken before and after cleaning
  • Design of validation protocols and reports  

 

Why choose Eurofins BioPharma Product Testing Netherlands?

  • Single point of contact. Benefit from streamlined communication through a single local point of contact while leveraging the advantages of our extensive global network.
  • Complete service portfolio. Leveraging our network of GMP product testing laboratories, we can offer a comprehensive testing service portfolio to our customers.
  • Standard and custom solutions. If our standard methods do not meet your needs, our skilled technicians can develop customised testing methods tailored to your specific requirements.

Please contact us if you want to discuss your needs.