Validation is the one of the most important step in achieving and maintaining the quality of the final product. Validation is defined as the collection and evaluation of the data from process design stages through production which establishes scientific evidence that a process is capable of consistently delivering quality product. If each step of the production process is validated than one can assure the final product is of the best quality. Validation of individual step is called as process validation. The purpose of the research was to study Prospective process validation of Piroxicam Dispersible tablet 20mg. In this article three batches of Piroxicam Dispersible Tablets were taken. They have same size, quantity, equipment, method and validation criteria. The critical parameters involved in sifting, milling, blending, lubrication and compression were identified and evaluated as per Validation Master Plan. All batches fulfill the requirement of given criteria. The outcome states that this Process Validation gives a higher degree of quality assurance.
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