Systematical approach in evaluation of LC method for determination of raloxifene hydrochloride and its impurities employing experimental design
Method validation presents a detailed investigation of analytical method and provision of the evidence that the method, when correctly applied, produces results that fit to the purpose. In order to achieve the method validation scope efficiently, experimental design presents a very useful tool. The...
Saved in:
Main Authors: | B. JanÄiÄ StojanoviÄ (Author), T. RakiÄ (Author), B. SlavkoviÄ (Author), N. KostiÄ (Author), A. VemiÄ (Author), A. MalenoviÄ (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2013-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
LC-UV method to assay raloxifene hydrochloride in rat plasma and its application to a pharmacokinetic study
by: Márcia Camponogara Fontana, et al. -
Synthesis, isolation, identification and characterization of new process-related impurity in isoproterenol hydrochloride by HPLC, LC/ESI-MS and NMR
by: Neeraj Kumar, et al.
Published: (2017) -
First Report of Erythema Multiforme Minor Caused by Raloxifene Hydrochloride
by: Yurie Norimatsu, et al.
Published: (2021) -
Development of alternative methods for the determination of raloxifene hydrochloride in tablet dosage form
by: Fernanda Rodrigues Salazar, et al.
Published: (2015) -
Development and Evaluation of Raloxifene-Hydrochloride-Loaded Supersaturatable SMEDDS Containing an Acidifier
by: Jong-Hwa Lee, et al.
Published: (2018)