Bio Process >> Residuals Testing and Process related impurities >> Endotoxins

Endotoxins

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Injectable therapeutics and medical devices placed inside the body need to be verifiably free from endotoxins to ensure patient safety. To ensure this, current GMP regulations require that final products and in some cases raw materials need to be tested for endotoxins prior to their use. At Eurofins BioPharma Product Testing Netherlands we have more then 15 years of experience in endotoxin testing, and can offer you the highest quality service and expertise.

Where to test for endotoxin?

Guidelines proscribe endotoxin testing at various stages of production, including but not limited to:

  • Raw material
  • Bulk harvest
  • Final Product

How is endotoxin testing performed?

There are several endotoxin testing methods available. We offer the following endotoxin tests in house:

  • Gel-clot (LAL test)
  • Kinetic Chromogenic methods (USP Chromogenic)
  • Kinetic Turbidimetric method

We are expert in all three types of endotoxin tests and can use our expertise to ensure your samples are tested using the most appropriate method.

Are you looking for more detailed information about the tests? Contact us and we help you decide which options is best for you.