• Anand Sabne
• Mahesh Sontakke
• Vaishnavi Rathi
• Sachin Gholve

The ability to effectively create and put into practice the specified procedures while using documentation is known as "validation." Process validation gives evidence that a certain method produces a product that also complies with specified requirements and quality criteria. Validation of the drug product's manufacturing method, from formulation development to the final commercial batch. Developing a method for the portion of the pharmacy industry that is interested in the finished product or process tests, going to prepare samples, and offering a practical method for estimating the selectivity, specificity, quantity limit detection, linearity, the accuracy of the range, precision, consistency of the recovery solution, robustness, and robustness of liquid chromatographic methods are all part of this process. Therefore, legality is a crucial part of pharmaceutical chemistry and quality control.

Standard Operating Procedures, Process Qualification, Operational Qualification, Limit of Quantification, Limit of Detection.

"PHARMACEUTICAL VALIDATION: A REVIEW ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.10, Issue 4, page no.589-599, April-2023, Available :http://www.jetir.org/papers/JETIRFW06080.pdf

"PHARMACEUTICAL VALIDATION: A REVIEW ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.10, Issue 4, page no. pp589-599, April-2023, Available at : http://www.jetir.org/papers/JETIRFW06080.pdf