Loading component...
Loading component...
Loading component...
Process-related impurities and residual analysis from SGS – effective residual impurity testing and residual analysis for your biopharmaceutical products.
Process-related impurities and residual analysis from SGS – effective residual impurity testing and residual analysis for your biopharmaceutical products.
A variety of compounds added during the manufacture of your biopharmaceutical products can appear in the final product as process-related impurities. However, residual impurities can be difficult to detect. That’s why we offer you effective process related impurities analysis, residual impurity testing and residual analysis in biopharmaceuticals. As a result, we can help you to confirm the efficient removal of impurities by the downstream process and absence from the final product.
We offer process-related impurities analysis, residual impurity testing and residual analysis in biopharmaceuticals to help you:
As the world’s leading provider of residual impurity testing and residual analysis in biopharmaceuticals, we provide you with the experience, technical and regulatory expertise, and unique global network you need.
We offer you a wide range of state-of-the-art chromatography and mass spectrometry instrumentation, together with extensive method development experience, which are utilized in the optimization of the analytical method for the analysis of impurities. The optimized method can then be validated either as a limit test or full ICH Q2(R1) validation performed under GMP.
To find out more about our process related impurities analysis services, contact us today.
2nd Floor Alegria Office Building. 2229 Chino Roces Avenue,
1223,
Makati, Metro Manila, Philippines