Pharma

INTERLABOR gladly supports you in quality control. Whether for the analysis of raw materials according to monographs or general pharmacopoeia methods or for the analysis of intermediate and finished products according to customer procedures: We are at your disposal. Furthermore, we also develop new methods or conduct stability studies according to ICH guidelines or special guidelines. Depending on the customer‘s requirements, the results are prepared according to GMP guidelines, including the necessary development, validation or verification analytics. Thanks to decades of analytical experiences combined with a well-equipped instruments pool and an established Q-system, INTERLABOR can offer a comprehensive range of services for the pharmaceutical industry:     

  • Analysis of raw materials according to common pharmacopoeias (Ph.Eur, USP etc.)
  • Analysis of intermediate and finished products by validated methods
  • Validation and transfer of analysis methods
  • Stability studies according to ICH Q1 inclusive photo stability according to ICH Q1B
  • Development of stability indicating methods
  • Identification and isolation of unknown degradation products and impurities
  • Extractables and leachables studies for various packaging and product materials
  • Development of analysis methods for cleaning and process validations (swabs, rinsing agents etc.)
  • Analysis of foreign matter
  • Analysis of residues and contaminants (pesticides, heavy metals, toxins, aflatoxin B1 et ochratoxin A according to Ph.Eur, USP etc.)
  • Performance of antimicrobial effectiveness testing (Ph.Eur, USP etc.)

OUR CONSULTING SERVICES

If you have any questions or require further information, please feel free to browse through our FAQ section or contact our customer advisors directly.


Your contact persons for pharmaceutical analytics

Dr. Olivier Aebischer

Head of Customer Service

Dr. Simone Szymanski

Customer Advisor

Martina Lingg

Customer Advisor


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