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Author(s): Laxmi S. Vasave*1, Prajakta G. Chavan2, Sakshi K. Chaudhari3, Sunila A. Patil4, Sunil P. Pawar5

Email(s): 1laxmivasave22@gmail.com

Address:

    Department of Quality Assurance, P. S. G. V. P. Mandal’s College of Pharmacy, Shahada.

Published In:   Volume - 2,      Issue - 4,     Year - 2023

DOI: Not Available

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ABSTRACT:
The development of good analytical method is of highest importance during the process of drug discovery, launch to market, and development, which results in a marketing authorization. The objective of this study is to assess the technique development, standardization, and validation for the drug from the early phases of formulation establishment through its first batch for commercial sale. Development of a method for the required element in process testing, a sample, or the final product to simplify the process of developing pharmaceuticals and to offer useful methods for assessing the selectivity, specificity, limits of detection and quantification, linearity, range accuracy, precision, and stability of the recovery solution. Also liquid chromatography offers durability and ruggedness of procedures to allow regular, in-process, and stability evaluation.

Cite this article:
Laxmi S. Vasave*, Prajakta G. Chavan, Sakshi K. Chaudhari, Sunila A. Patil, Sunil P. Pawar. Review on: Analytical method development and validation. IJRPAS, May-June 2023; 2(3): 10-18.


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