• Priyanka Jha
• Mrs. Sunita Arya
• Miss Gulbahar

Process Validation in pharmaceuticals is one of the important steps in accomplishing and maintaining the quality of final product. It gives a higher degree of assurance of pharmaceutical product. Validation simply can be described as documented practice which delivers the evidence that any of the equipment process, procedure, material, procedure and system truly shows the predetermined result. Process validation is expressed as the practice which involves the selection and estimation of data during the different phases of pharmaceutical activities, starting from the procedure design phase during the production process and establishing the scientific indication that a procedure is manufacturing quality outcomes. In process supervising of critical processing phases and product testing lies under this validation which assist to produce the documented evidence showing the manufacturing procedure is proceed under a suitable state of control with quality characteristics. The validated documentation obtained from the concurrent process validation can be further used in the future to perform the retrospective process validation for the reference purpose.

Validation, Process validation, Concurrent Process Validation

"A Review Article On concurrent process validation of solid Dosages form", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.9, Issue 2, page no.a335-a341, February-2022, Available :http://www.jetir.org/papers/JETIR2202042.pdf

"A Review Article On concurrent process validation of solid Dosages form", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.9, Issue 2, page no. ppa335-a341, February-2022, Available at : http://www.jetir.org/papers/JETIR2202042.pdf