The Main Components of Pharmaceutical Process Validation

Bin Guo

doi:10.4172/2167-065X.1000284

ISSN: 2167-065X

Clinical Pharmacology & Biopharmaceutics
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DOI: 10.4172/2167-065X.1000284

The Main Components of Pharmaceutical Process Validation

Bin Guo^*: Department of Pharmaceutical Sciences, North Dakota State University, USA

^*Corresponding Author : Bin Guo, Department of Pharmaceutical Sciences, North Dakota State University, USA, Email: Bin_Guo@gmail.com

Received Date: Aug 01, 2022 / Accepted Date: Aug 31, 2022 / Published Date: Aug 31, 2022

Abstract

Process Confirmation in Manufacturing of Biopharmaceuticals, Third Edition delves into the crucial aspects and current practices of process confirmation. It includes discussion on the final interpretation of the FDA 2011 Guidance for Assiduity on Process Validation Principles and Practices, generally appertained to as the Process Validation Guidance or PVG, issued in final form on January 24, 2011.

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Citation: Guo B (2022) The Main Components of Pharmaceutical Process Validation. Clin Pharmacol Biopharm, 11: 284. Doi: 10.4172/2167-065X.1000284

Copyright: © 2022 Guo B. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Clinical Pharmacology & Biopharmaceutics
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