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 over 15 years of experience in endotoxin testing, and offer the highest quality service and expertise.
When to test for endotoxin?
Guidelines advise endotoxin testing at various stages of production, including but not limited to:
- Raw material
- Bulk harvest
- Final Product
What do we offer?
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 use our extensive knowledge to ensure your samples are tested using the most appropriate method.
Why choose Eurofins BioPharma Product Testing Netherlands
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Great flexibility. Our focus on small scale projects allows all flexibility you need.
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Single-point-of-contact. With a wide array of services internally available, all communication is centralized.
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Complete service portfolio. Many additional chemical, microbiological and ancillary services performed in GMP certified, WHO prequalified and FDA approved labs.
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Standard and custom solutions. If our standard solutions do not fulfill your requirements, our skilled technicians are able to develop specialized solutions. Please contact us if you want to discuss your needs.
If you want to discuss your project or request a quotation, feel free to contact us.
