• Neha shah
• SUNITA ARYA
• SONI MATELA
• Dr. Praveen Kumar Ashok

Validation is widely recognized as a crucial parameter in Good Manufacturing Practices (GMP). The process validation of pharmaceutical manufacturing processes is of significant importance, aiming to ensure the reproducible quality of drugs. This study provides an overview of process validation, emphasizing the need to build quality into every stage of production rather than relying solely on end-product testing. Process validation, in line with ISO 9000:2000, serves as a vital tool for quality management in the pharmaceutical industry. It is conducted before product release, during product changes, and continuously to verify the proper functioning of the process. A well-defined protocol should be established, outlining monitored parameters, sample collection, and acceptance criteria for results.

Process validation, Quality, Protocol, Quality Management, Voriconazole

"Concurrent Process Validation of Voriconazole Tablets IP 200 mg", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.10, Issue 6, page no.d947-d954, June-2023, Available :http://www.jetir.org/papers/JETIR2306425.pdf

"Concurrent Process Validation of Voriconazole Tablets IP 200 mg", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.10, Issue 6, page no. ppd947-d954, June-2023, Available at : http://www.jetir.org/papers/JETIR2306425.pdf