Analytical and Chemical Development
Agilent experts transfer, develop, qualify, and validate analytical methods from investigational new drug (IND) to new drug application (NDA) and biologics license application (BLA). Agilent finds to positively identify impurities and uses quantitative mass spectrometry for critical impurities.
Ensuring safety and robustness, Agilent experts scale chemical processes from grams to tens of kilograms. The Agilent development team will support you with process optimization, scaling, and validation to deliver high-quality material throughout your active pharmaceutical ingredient (API) development cycle.
Ensuring safety and robustness, Agilent experts scale chemical processes from grams to tens of kilograms. The Agilent development team will support you with process optimization, scaling, and validation to deliver high-quality material throughout your active pharmaceutical ingredient (API) development cycle.