Neugen labs has extensive experience in Analytical Method Devolopment, Method Validation, Method Transfer. Method development is the process of proving that an analytical method is acceptable for use in our laboratory to measure the concentra*’ f an API in a specific compounded dosage form.
For established pharmaceutical preparations, which are not new drug speci‹ analytical method process can be much simpler. Majority of analytical m- —
developed ai e by using volatile buffers which facilitate the structuie elucidation LC- MS Studies .Modern analytical instrumentation, like high performance chromatography with versatile detectors such as the ultraviolet ,photodiodr
spectrometer (HPLC- PDA), allow simplified procedures to be employed to verify that an analysis procedure accurately and consistently will deliver a reliable measurement of an active ingredient in a compounded preparation.