PHARMACEUTICAL PROCESS VALIDATION OF SOLID DOSAGE FORMS: A REVIEW
The concept of validation was first proposed by Food and Drug Administration officials in 1970 in order to improve the quality of pharmaceuticals. Process validation is the key element in assurance of pharmaceutical product. It is the most important and recognized parameters of cGMP. T his establishes the flexibility and strict quality control in the manufacturing process control in the attainment of desirable attributes in the drug products while preventing undesirable properties. Throu gh this review the authors make an effort to explai n, the overview of validation concept of conducting validation trials and provide an insight to its importance in the pharmaceutical industry