Review Article
Development and Validation of Analytical Methods for Pharmaceuticals
Nishant Toomula1*, Arun Kumar2, Sathish Kumar D3 and Vijaya Shanti Bheemidi41Department of Biotechnology, GITAM Institute of Technology, GITAM University, Visakhapatnam, India
2Department of Biochemistry, GITAM University, Visakhapatnam, India
3Department of Biotechnology, University of Hyderabad, Hyderabad, India
4Department of Biotechnology, Nottingham Trent University, Nottingham, United Kingdom
- *Corresponding Author:
- Nishant Toomula
Department of Biotechnology
GITAM Institute of Technology, GITAM University
Visakhapatnam, India
E-mail : nishanththumula@gmail.com
Received date: October 15, 2011; Accepted date: December 02, 2011; Published date: December 06, 2011
Citation: Nishant T, Arun Kumar, Sathish Kumar D, Vijaya Shanti B (2011) Development and Validation of Analytical Methods for Pharmaceuticals. J Anal Bioanal Tech 2:127. doi: 10.4172/2155-9872.1000127
Copyright: © 2011 Nishant T, et al. 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.
Abstract
Analytical methods development and validation play important roles in the discovery, development, and manufacture of pharmaceuticals. The official test methods that result from these processes are used by quality control laboratories to ensure the identity, purity, potency, and performance of drug products. This review gives information regarding various stages involved in development and validation of analytical methods like LC, HPLC, MS.
