STABILITY STUDY OF DOSAGE FORM: AN INOVATIVE STEP
Thorat Punam*, Warad Shubhangi, Solunke Rahul, Ashok Sargar, Anagha Bhujbal,
Asha Shinde.
ABSTRACT
Stability studies ensuring the maintenance of product quality, safety
and efficacy throughout the shelf life are considered as pre-requisite
for the acceptance and approval of any pharmaceutical product.
Stability testing is a routine procedure performed on drug substances
and products and is employed at various stages of the product
development. Importance of various methods followed for stability
testing of pharmaceutical products, guidelines issued for stability
testing and other aspects related to stability of pharmaceutical products
have been presented in a concise manner in the present review.
Stability of different pharmaceutical dosage forms is studies. Dosage
forms in which include the suspension, emulsion, aerosols, solid
dosage form, ointment, creams, capsules & other. Stability data innovative to prove the
quality of the product till expiry & Evaluation of quality. Stability of Pharmaceutical Product
Capacity of a drug substance or drug product in a given packaging system to remain within
established specifications to maintain its Quality (identity, strength, purity/impurity, potency)
and deliver the desired Performance throughout the retest or expiration period.
Keywords: Stability, Stability studies, Stability testing, suspension, emulsion, aerosols, ointment, creams, capsule.
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