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Eurofins Biopharma Product Testing Finland >> Our Services >> Development & validation of analytical methods

Development & Validation of Analytical Methods

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This service can be performed separately or as a part of your formulation development project. Over the years, we have assisted more than 60 clients in 300 projects.

Our service portfolio includes:

  • Method development, validation and transfer with full documentation
  • Development and validation of analytical methods for cleaning validation
  • Risk-based verification tests for pharmacopoeia methods.

Our humidity - and temperature-controlled GMP - certified laboratory is ideal for performing analytics for inhalation drug products in the required conditions. We have extensive experience in the development and validation of analytical methods of dry powder inhalers (DPIs), metered-dose inhalers (MDIs) and nebulisers.


Discover our full Inhalation Analytics offering here

 

Techniques for chemical and physical testing

  • UHPLCs with UV and PDA/DAD detectors
  • HPLCs with UV, PDA/DAD and RI detectors
  • GC with head space, FID detector
  • FTIR (FT infrared spectrometer)
  • Spectrophotometer
  • Polarimeter
  • Titrators
  • In vitro dissolution
  • Disintegration tester
  • Friability tester

If you’re interested in working with Eurofins on a Biopharma project, fill out the form below and a member of our Team will be in contact to discuss your project.

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