Analytical Method Validation for Assay Method (By UV) of Trypsin-Chymotrypsin Tablets 50000 AU of Enzymatic Activity

Authors

  • Dinesh Singh Research Scholar, Department of Pharmaceutical Chemistry, Shrinathji Institute of Pharmacy, Upali Oden, Nathdwara, Dist-Rajsamand (Raj.)-313301 India
  • D. B. Joshi Professor, Department of Pharmaceutical Chemistry, Shrinathji Institute of Pharmacy, Upali Oden, Nathdwara, Dist-Rajsamand (Raj.)-313301 India
  • R. S. Bhadauria Principal, Department of Pharmaceutical Chemistry, Shrinathji Institute of Pharmacy, Upali Oden, Nathdwara, Dist-Rajsamand (Raj.)-313301 India

Keywords:

Analytical method validation, Pharmaceutical analysis, Specificity, Precision, Accuracy

Abstract

It is internationally recognized that validation is necessary in analytical laboratories. The use of validated methods is important for an analytical laboratory to show its qualification and competency. When analytical method is utilized to generate results about the characteristics of drug related samples it is essential that the results are trustworthy. They may be utilized as the basis for decisions relating to administering the drug to patients. Analytical method validation required during drug development and manufacturing and these analytical methods are fit for their intended purpose. The purpose of this validation is to show that processes involved in the analytical testing can be performed in an effective and reproducible manner. This article provides a good, complete, up-to-date collation of relevant information in the fields of analytical method validation of Trypsin-Chymotrypsin Tablets 50000 AU of  Enzymatic Activity.

Keywords: Analytical method validation, Pharmaceutical analysis, Specificity, Precision, Accuracy.

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Published

2022-12-01

Issue

Vol. 10 No. 6 (2022): November-December

Section

Articles