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We, as pharmaceutical scientists, have always seen stability testing as a vital part of any drug development process. From the very basic level of experimentation, like stability of suspensions and emulsions in undergraduate laboratory, to stability testing of active pharmaceutical ingredients and conventional products containing them, and further to highly technical novel drug delivery systems, a thorough investigation on stability of every kind of product is desired for the benefit of the patients. Every product is supposed to be labeled with a valid expiry date and storage conditions, which are established through systematic stability studies. Due to many product failures and recalls happening for the reasons of instability, carrying out a successful stability program in the pharmaceutical industry has become very vital. Stability testing hence has to be a very well-organized activity, supported with due resources, which even stands up to critical regulatory scrutiny.
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