• Manish Kumar
• Dr. Praveen Kumar Ashok
• Gulfsha Parveen

The purpose of this process validation (Process performance Qualification) of the Carbamazepine Extended Release Tablets USP 100 mg is to establishing documented evidence to ensure that the process is feasible and to demonstrate that the product is producing a product meeting its predetermined process parameter requirements as per predefined product and quality attributes by collection and evaluation of the data from the manufacturing of tablets specification and quality attributes. During the work critical material attributes, critical process parameters are checked and controlled to achieve the desired critical quality attributes. The three consecutive batches are taken to validate the process. The manufacturing of the batch is done through wet Granulation technology.

PROCESS PERFORMANCE QUALIFICATION OF THE CARBAMAZEPINE EXTENDED RELEASE TABLETS USP 100 mg

"PROCESS PERFORMANCE QUALIFICATION OF THE CARBAMAZEPINE EXTENDED RELEASE TABLETS USP 100 mg", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.9, Issue 8, page no.c5-c28, August-2022, Available :http://www.jetir.org/papers/JETIR2208202.pdf

"PROCESS PERFORMANCE QUALIFICATION OF THE CARBAMAZEPINE EXTENDED RELEASE TABLETS USP 100 mg", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.9, Issue 8, page no. ppc5-c28, August-2022, Available at : http://www.jetir.org/papers/JETIR2208202.pdf