Pharmaffiliates 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 concentration
of an API in a specific compounded dosage form.
For established pharmaceutical preparations, which are not new drug species, the
analytical method process can be much simpler. Majority of analytical methods developed
are by using volatile buffers which facilitate the structure elucidation during
LC-MS Studies .Modern analytical instrumentation, like high performance liquid chromatography
with versatile detectors such as the ultraviolet ,photodiode array 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.